A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16944264



Internal ID30177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196485909..196486542hg38UCSC Ensembl
chr3:196212780..196213413hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437996
Supporting Variants
Samples
Known GenesRNF168
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16944264
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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