A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687761



Internal ID15077727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29942474..29991339hg38UCSC Ensembl
Innerchr9:29942472..29991337hg19UCSC Ensembl
Innerchr9:29932472..29981337hg18UCSC Ensembl
Innerchr9:29932472..29981337hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3848866
hg1948866
hg1848866
hg1748866
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517063
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687761
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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