A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522670



Internal ID15449963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76174277..76185528hg38UCSC Ensembl
Innerchr11:75885321..75896572hg19UCSC Ensembl
Innerchr11:75562969..75574220hg18UCSC Ensembl
Innerchr11:75562969..75574220hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3811252
hg1911252
hg1811252
hg1711252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706075
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522670
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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