A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4013882



Internal ID22075513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:24438155..24444068hg38UCSC Ensembl
Outerchr20:24434641..24446774hg38UCSC Ensembl
Innerchr20:24418791..24424704hg19UCSC Ensembl
Outerchr20:24415277..24427410hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3812134
hg1912134
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155651
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4013882
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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