A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938944



Internal ID26682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145721613..145779463hg38UCSC Ensembl
chr3:145439400..145497250hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3857851
hg1957851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5434341
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938944
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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