A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1040405



Internal ID15893591
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 StatusS
Merged Variantsnsv599409
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1040405
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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