A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1039628



Internal ID15892814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:101995609..102103966hg38UCSC Ensembl
Innerchr5:101331313..101439670hg19UCSC Ensembl
Innerchr5:101359212..101467569hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38108358
hg19108358
hg18108358
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599187
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)nssv1039628
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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