A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699420



Internal ID15089386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:94233701..94285237hg38UCSC Ensembl
Innerchr15:94776930..94828466hg19UCSC Ensembl
Innerchr15:92577934..92629470hg18UCSC Ensembl
Innerchr15:92577934..92629470hg17UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3851537
hg1951537
hg1851537
hg1751537
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523623
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699420
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