A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv765363



Internal ID16059319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5361785..5362568hg38UCSC Ensembl
Innerchr11:5383015..5383798hg19UCSC Ensembl
Innerchr11:5339591..5340374hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38784
hg19784
hg18784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553237
Supporting Variants
Samples
Known GenesOR51B5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv765363
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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