A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524707



Internal ID15452000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:84514467..84547446hg38UCSC Ensembl
Innerchr9:87129382..87162361hg19UCSC Ensembl
Innerchr9:86319202..86352181hg18UCSC Ensembl
Innerchr9:84358936..84391915hg17UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3832980
hg1932980
hg1832980
hg1732980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700690
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524707
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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