A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156876



Internal ID22087277
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv281n97
Supporting Variantsnssv4020968
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156876
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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