A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv599656



Internal ID16387065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:124534167..124584238hg38UCSC Ensembl
Innerchr5:123869860..123919931hg19UCSC Ensembl
Innerchr5:123897759..123947830hg18UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3850072
hg1950072
hg1850072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153996
Samples1782681195_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv599656
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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