A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596892



Internal ID16384301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1832126..1892645hg38UCSC Ensembl
Innerchr5:1832240..1892759hg19UCSC Ensembl
Innerchr5:1885240..1945759hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3860520
hg1960520
hg1860520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9542n54
Supporting Variantsnssv1022209
Samples
Known GenesIRX4, LOC101929034
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596892
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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