A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4020947



Internal ID22082578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15465904..15474556hg38UCSC Ensembl
Outerchr8:15460281..15477834hg38UCSC Ensembl
Innerchr8:15323413..15332065hg19UCSC Ensembl
Outerchr8:15317790..15335343hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3817554
hg1917554
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156867
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4020947
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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