A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526579



Internal ID15107186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113482702..113628882hg38UCSC Ensembl
Innerchr9:116244982..116391162hg19UCSC Ensembl
Innerchr9:115284803..115430983hg18UCSC Ensembl
Innerchr9:113324536..113470716hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38146181
hg19146181
hg18146181
hg17146181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702897
Samples
Known GenesRGS3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526579
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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