A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518879



Internal ID15446172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:74908774..74930322hg38UCSC Ensembl
Innerchr9:77523690..77545238hg19UCSC Ensembl
Innerchr9:76713510..76735058hg18UCSC Ensembl
Innerchr9:74753244..74774792hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3821549
hg1921549
hg1821549
hg1721549
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696336
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518879
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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