A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528261



Internal ID15455554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:58636360..58637260hg38UCSC Ensembl
Innerchr11:58403833..58404733hg19UCSC Ensembl
Innerchr11:58160409..58161309hg18UCSC Ensembl
Innerchr11:58160409..58161309hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38901
hg19901
hg18901
hg17901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv70n21
Supporting Variantsnssv704828
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528261
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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