A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4020968



Internal ID22082599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:20306406..20390975hg38UCSC Ensembl
Outerchr8:20296439..20397135hg38UCSC Ensembl
Innerchr8:20163917..20248486hg19UCSC Ensembl
Outerchr8:20153950..20254646hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38100697
hg19100697
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156876
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4020968
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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