A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600293



Internal ID16387702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:172715548..172761210hg38UCSC Ensembl
Innerchr5:172142551..172188213hg19UCSC Ensembl
Innerchr5:172075156..172120818hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3845663
hg1945663
hg1845663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10174n54
Supporting Variantsnssv1045484
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600293
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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