A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518887



Internal ID15099494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94979681..94983834hg38UCSC Ensembl
Innerchr11:94712845..94716998hg19UCSC Ensembl
Innerchr11:94352493..94356646hg18UCSC Ensembl
Innerchr11:94352493..94356646hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg384154
hg194154
hg184154
hg174154
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696346
Samples
Known GenesKDM4D
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518887
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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