A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1040247



Internal ID15893433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:110823895..111029119hg38UCSC Ensembl
Innerchr5:110159594..110364818hg19UCSC Ensembl
Innerchr5:110187493..110392717hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg38205225
hg19205225
hg18205225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599356
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)nssv1040247
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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