A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700690



Internal ID15437342
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524707
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700690
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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