A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598409



Internal ID16385818
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 StatusM
Merged Variantsdgv9830n54
Supporting Variantsnssv1153358
SamplesHGDP00064
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598409
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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