A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv776582



Internal ID15723852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55607522..55639688hg38UCSC Ensembl
Innerchr11:55374998..55407164hg19UCSC Ensembl
Innerchr11:55131574..55163740hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3832167
hg1932167
hg1832167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554926
Supporting Variants
Samples
Known GenesOR4P4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv776582
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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