A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520760



Internal ID15101367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69420931..69433561hg38UCSC Ensembl
Innerchr9:72035847..72048477hg19UCSC Ensembl
Innerchr9:71225667..71238297hg18UCSC Ensembl
Innerchr9:69265401..69278031hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3812631
hg1912631
hg1812631
hg1712631
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv675046, nssv680064
Samples
Known GenesAPBA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520760
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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