A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553151



Internal ID16340560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4164365..4251113hg38UCSC Ensembl
Innerchr11:4185595..4272343hg19UCSC Ensembl
Innerchr11:4142171..4228919hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3886749
hg1986749
hg1886749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174289
SamplesHGDP01339
Known GenesLOC100506082
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553151
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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