A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522776



Internal ID15103383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132949989..132958940hg38UCSC Ensembl
Innerchr11:132819884..132828835hg19UCSC Ensembl
Innerchr11:132325094..132334045hg18UCSC Ensembl
Innerchr11:132325094..132334045hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg388952
hg198952
hg188952
hg178952
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698417
Samples
Known GenesOPCML
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522776
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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