A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521775



Internal ID15102382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:117471092..117482288hg38UCSC Ensembl
Innerchr11:117341808..117353003hg19UCSC Ensembl
Innerchr11:116847018..116858213hg18UCSC Ensembl
Innerchr11:116847018..116858213hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3811197
hg1911196
hg1811196
hg1711196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694541
Samples
Known GenesDSCAML1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521775
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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