A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv775973



Internal ID15723243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55631424hg38UCSC Ensembl
Innerchr11:55371021..55398900hg19UCSC Ensembl
Innerchr11:55127597..55155476hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3827880
hg1927880
hg1827880
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554885
Supporting Variants
Samples
Known GenesOR4C11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv775973
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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