A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596907



Internal ID16384316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2052987..2066051hg38UCSC Ensembl
Innerchr5:2053101..2066165hg19UCSC Ensembl
Innerchr5:2106101..2119165hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3813065
hg1913065
hg1813065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9545n54
Supporting Variantsnssv1023658
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596907
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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