A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695459



Internal ID15432111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4750269..4787987hg38UCSC Ensembl
Innerchr9:4750269..4787987hg19UCSC Ensembl
Innerchr9:4740269..4777987hg18UCSC Ensembl
Innerchr9:4740269..4777987hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3837719
hg1937719
hg1837719
hg1737719
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518048
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695459
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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