A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709133



Internal ID132799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75627169..75627220hg38UCSC Ensembl
chr16:75661067..75661118hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538520
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709133
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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