A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145328



Internal ID344533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4706000..4712000hg38UCSC Ensembl
chr16:4756001..4762001hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704822
Samples
Known GenesANKS3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145328
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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