A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700519



Internal ID15437171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23078403..23081307hg38UCSC Ensembl
Innerchr9:23078402..23081306hg19UCSC Ensembl
Innerchr9:23068402..23071306hg18UCSC Ensembl
Innerchr9:23068402..23071306hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg382905
hg192905
hg182905
hg172905
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521195
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700519
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