A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156880



Internal ID22087281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:20326828..20380399hg38UCSC Ensembl
Outerchr8:20323181..20380506hg38UCSC Ensembl
Innerchr8:20184339..20237910hg19UCSC Ensembl
Outerchr8:20180692..20238017hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3857326
hg1957326
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4020973
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156880
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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