A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524659



Internal ID15451952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19881266..20016780hg38UCSC Ensembl
Innerchr9:19881264..20016778hg19UCSC Ensembl
Innerchr9:19871264..20006778hg18UCSC Ensembl
Innerchr9:19871264..20006778hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38135515
hg19135515
hg18135515
hg17135515
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv481n21
Supporting Variantsnssv700626
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524659
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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