A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939987



Internal ID27378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132945787..132951574hg38UCSC Ensembl
chr3:132664631..132670418hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg385788
hg195788
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139900
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939987
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.007108


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