A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519360



Internal ID15446653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:117026851..117125298hg38UCSC Ensembl
Innerchr9:119789130..119887577hg19UCSC Ensembl
Innerchr9:118828951..118927398hg18UCSC Ensembl
Innerchr9:116868684..116967131hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3898448
hg1998448
hg1898448
hg1798448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696810
Samples
Known GenesASTN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519360
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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