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GRCh38/hg38 16p11.2(chr16:29581462-29720976)x4 AND See cases

Significance: Likely benign
ClinVar: RCV000140294

Variant: GRCh38/hg38 16p11.2(chr16:29581462-29720976)x4

Type: Variant
Allele: GRCh38/hg38 16p11.2(chr16:29581462-29720976)x4 161340
Gene:
Type: copy number gain
Location: Chr16: 29592783 - 29732297 - assembly GRCh37
Chr16: 29500284 - 29639798 - assembly NCBI36
Chr16: 29581462 - 29720976 - assembly GRCh38
Chr16: 29581462 - 29720976 - assembly GRCh38
References: dbVar: nsv931477
dbVar: nssv1609464

Condition

PhenotypeInstruction: See cases