A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv599409



Internal ID16386818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:113743657..113848514hg38UCSC Ensembl
Innerchr5:113079354..113184211hg19UCSC Ensembl
Innerchr5:113107253..113212110hg18UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38104858
hg19104858
hg18104858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10012n54
Supporting Variantsnssv1040405
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv599409
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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