A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv774766



Internal ID15722036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54928232..55290722hg38UCSC Ensembl
Innerchr11:54695707..55058198hg19UCSC Ensembl
Innerchr11:54452283..54814774hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38362491
hg19362492
hg18362492
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554617
Supporting Variants
Samples
Known GenesTRIM48
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv774766
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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