A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153358



Internal ID15872876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:67827709..67889394hg38UCSC Ensembl
Innerchr5:67123537..67185222hg19UCSC Ensembl
Innerchr5:67159293..67220978hg18UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg3861686
hg1961686
hg1861686
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598409
Supporting Variants
SamplesHGDP00064
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153358
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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