A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526162



Internal ID15106769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61090559..61111190hg38UCSC Ensembl
Innerchr11:60858031..60878662hg19UCSC Ensembl
Innerchr11:60614607..60635238hg18UCSC Ensembl
Innerchr11:60614607..60635238hg17UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3820632
hg1920632
hg1820632
hg1720632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702421
Samples
Known GenesCD5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526162
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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