A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931122



Internal ID21498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15254095..15254095hg38UCSC Ensembl
chr3:15295602..15295602hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5548395
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931122
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000313


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