A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662583



Internal ID15399235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2731748..2734038hg38UCSC Ensembl
Innerchr9:2731748..2734038hg19UCSC Ensembl
Innerchr9:2721748..2724038hg18UCSC Ensembl
Innerchr9:2721748..2724038hg17UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg382291
hg192291
hg182291
hg172291
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516425
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662583
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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