A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598389



Internal ID16385798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:64414728..64499640hg38UCSC Ensembl
Innerchr5:63710555..63795467hg19UCSC Ensembl
Innerchr5:63746311..63831223hg18UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3884913
hg1984913
hg1884913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9819n54
Supporting Variantsnssv1153353
SamplesHGDP00774
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598389
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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