A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553059



Internal ID15993782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1883506..1886126hg38UCSC Ensembl
Innerchr11:1904736..1907356hg19UCSC Ensembl
Innerchr11:1861312..1863932hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382621
hg192621
hg182621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv764474
Samples
Known GenesLSP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553059
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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