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GRCh38/hg38 16p12.3-12.2(chr16:20408020-21244474)x1 AND See cases

Significance: Uncertain significance
ClinVar: RCV000139900

Variant: GRCh38/hg38 16p12.3-12.2(chr16:20408020-21244474)x1

Type: Variant
Allele: GRCh38/hg38 16p12.3-12.2(chr16:20408020-21244474)x1 160907
Gene:
Type: copy number loss
Location: Chr16: 20419342 - 21255795 - assembly GRCh37
Chr16: 20326843 - 21163296 - assembly NCBI36
Chr16: 20408020 - 21244474 - assembly GRCh38
Chr16: 20408020 - 21244474 - assembly GRCh38
References: dbVar: nsv931040
dbVar: nssv1608263

Condition

PhenotypeInstruction: See cases