A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688016



Internal ID15077982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5461379..5464065hg38UCSC Ensembl
Innerchr9:5461379..5464065hg19UCSC Ensembl
Innerchr9:5451379..5454065hg18UCSC Ensembl
Innerchr9:5451379..5454065hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg382687
hg192687
hg182687
hg172687
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519771
Supporting Variants
Samples
Known GenesCD274
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688016
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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