A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007589



Internal ID22069220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:10490122..10539812hg38UCSC Ensembl
Outerchr2:10484528..10547925hg38UCSC Ensembl
Innerchr2:10630248..10679938hg19UCSC Ensembl
Outerchr2:10624654..10688051hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3863398
hg1963398
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155158
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007589
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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