A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940051



Internal ID27417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156784763..156785385hg38UCSC Ensembl
chr3:156502552..156503174hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38623
hg19623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435722
Supporting Variants
Samples
Known GenesLINC00886
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940051
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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