A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702421



Internal ID15092387
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526162
Supporting Variants
Samples
Known GenesCD5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702421
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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