A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518815



Internal ID15099422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132529378..132534561hg38UCSC Ensembl
Innerchr11:132399272..132404455hg19UCSC Ensembl
Innerchr11:131904482..131909665hg18UCSC Ensembl
Innerchr11:131904482..131909665hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg385184
hg195184
hg185184
hg175184
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696268
Samples
Known GenesOPCML
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518815
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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