A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696241



Internal ID15432893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:36536513..36545979hg38UCSC Ensembl
Innerchr15:36828714..36838180hg19UCSC Ensembl
Innerchr15:34616006..34625472hg18UCSC Ensembl
Innerchr15:34616006..34625472hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg389467
hg199467
hg189467
hg179467
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518788
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696241
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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