A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020142



Internal ID19109361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:408606..491776hg38UCSC Ensembl
Innerchr8:358606..441776hg19UCSC Ensembl
Innerchr8:348606..431776hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3883171
hg1983171
hg1883171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674927
Samples
Known GenesFBXO25, TDRP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020142
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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