A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1040457



Internal ID15893643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:114604490..114670467hg38UCSC Ensembl
Innerchr5:113940187..114006164hg19UCSC Ensembl
Innerchr5:113968086..114034063hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3865978
hg1965978
hg1865978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599434
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)nssv1040457
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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