A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522884



Internal ID15450177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6123768..6143470hg38UCSC Ensembl
Innerchr11:6144998..6164700hg19UCSC Ensembl
Innerchr11:6101574..6121276hg18UCSC Ensembl
Innerchr11:6101574..6121276hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3819703
hg1919703
hg1819703
hg1719703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698540
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522884
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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