A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv774070



Internal ID16068026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54784245..54898271hg38UCSC Ensembl
Innerchr11:51221009..51335035hg19UCSC Ensembl
Innerchr11:51077585..51191611hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38114027
hg19114027
hg18114027
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554455
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv774070
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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