A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522721



Internal ID15103328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139632326..139643627hg38UCSC Ensembl
Innerchr8:140644569..140655870hg19UCSC Ensembl
Innerchr8:140713751..140725052hg18UCSC Ensembl
Innerchr8:140713751..140725052hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3811302
hg1911302
hg1811302
hg1711302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698352
Samples
Known GenesKCNK9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522721
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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