A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1124908



Internal ID15978094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:141905148..141967322hg38UCSC Ensembl
Innerchr8:142986509..143048683hg19UCSC Ensembl
Innerchr8:142984416..143046590hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3862175
hg1962175
hg1862175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612687
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)nssv1124908
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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