A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1125579



Internal ID15632079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143618479..143626978hg38UCSC Ensembl
Innerchr8:144700649..144709148hg19UCSC Ensembl
Innerchr8:144771792..144780291hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg388500
hg198500
hg188500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612863
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)nssv1125579
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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