A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528334



Internal ID15455627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:127286837..127328649hg38UCSC Ensembl
Innerchr11:127156732..127198544hg19UCSC Ensembl
Innerchr11:126661942..126703754hg18UCSC Ensembl
Innerchr11:126661942..126703754hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3841813
hg1941813
hg1841813
hg1741813
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704916
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528334
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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