A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1029099



Internal ID15535599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:37839834..37840407hg38UCSC Ensembl
Innerchr5:37839936..37840509hg19UCSC Ensembl
Innerchr5:37875693..37876266hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38574
hg19574
hg18574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597853
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)nssv1029099
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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