A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523683



Internal ID8417958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:113470669..113476233hg38UCSC Ensembl
Innerchr11:113341391..113346955hg19UCSC Ensembl
Innerchr11:112846601..112852165hg18UCSC Ensembl
Innerchr11:112846601..112852165hg17UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg385565
hg195565
hg185565
hg175565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699487
Samples
Known GenesDRD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523683
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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