A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521504



Internal ID15102111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132949989..132954476hg38UCSC Ensembl
Innerchr11:132819884..132824371hg19UCSC Ensembl
Innerchr11:132325094..132329581hg18UCSC Ensembl
Innerchr11:132325094..132329581hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg384488
hg194488
hg184488
hg174488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698121
Samples
Known GenesOPCML
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521504
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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