A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940662



Internal ID27813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141868869..141868984hg38UCSC Ensembl
chr3:141587711..141587826hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5441561
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940662
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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