A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933656



Internal ID23170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44629776..44629963hg38UCSC Ensembl
chr3:44671268..44671455hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442365
Supporting Variants
Samples
Known GenesZNF197
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933656
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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