A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600188



Internal ID16387597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:163321598..163376925hg38UCSC Ensembl
Innerchr5:162748604..162803931hg19UCSC Ensembl
Innerchr5:162681182..162736509hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3855328
hg1955328
hg1855328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10156n54
Supporting Variantsnssv1044955
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600188
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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