A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704278



Internal ID127944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65402519..65402569hg38UCSC Ensembl
chr15:65694857..65694907hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546741
Supporting Variants
Samples
Known GenesIGDCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704278
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002966


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer