A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519655



Internal ID15446948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8332388..8334366hg38UCSC Ensembl
Innerchr11:8353935..8355913hg19UCSC Ensembl
Innerchr11:8310511..8312489hg18UCSC Ensembl
Innerchr11:8310511..8312489hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381979
hg191979
hg181979
hg171979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696975
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519655
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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