A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520949



Internal ID15448242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:71778927..71795839hg38UCSC Ensembl
Innerchr9:74393843..74410755hg19UCSC Ensembl
Innerchr9:73583663..73600575hg18UCSC Ensembl
Innerchr9:71623397..71640309hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3816913
hg1916913
hg1816913
hg1716913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697704
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520949
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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