A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526086



Internal ID15453379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:72156123..72161733hg38UCSC Ensembl
Innerchr11:71867167..71872777hg19UCSC Ensembl
Innerchr11:71544815..71550425hg18UCSC Ensembl
Innerchr11:71544815..71550425hg17UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg385611
hg195611
hg185611
hg175611
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702330
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526086
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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