A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523078



Internal ID15450371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:13175491..13187828hg38UCSC Ensembl
Innerchr11:13197038..13209375hg19UCSC Ensembl
Innerchr11:13153614..13165951hg18UCSC Ensembl
Innerchr11:13153614..13165951hg17UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3812338
hg1912338
hg1812338
hg1712338
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698768
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523078
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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