A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523676



Internal ID15104283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38819509..38886797hg38UCSC Ensembl
Innerchr11:38841059..38908347hg19UCSC Ensembl
Innerchr11:38797635..38864923hg18UCSC Ensembl
Innerchr11:38797635..38864923hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3867289
hg1967289
hg1867289
hg1767289
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699480
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523676
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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