A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv776524



Internal ID15723794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55606497..55639307hg38UCSC Ensembl
Innerchr11:55373973..55406783hg19UCSC Ensembl
Innerchr11:55130549..55163359hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3832811
hg1932811
hg1832811
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554913
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)nssv776524
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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