A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526282



Internal ID15453575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38230635..38379666hg38UCSC Ensembl
Innerchr11:38252185..38401216hg19UCSC Ensembl
Innerchr11:38208761..38357792hg18UCSC Ensembl
Innerchr11:38208761..38357792hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38149032
hg19149032
hg18149032
hg17149032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702561
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526282
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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