A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155190



Internal ID22085695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:16845507..16854442hg38UCSC Ensembl
Outerchr2:16842485..16856053hg38UCSC Ensembl
Innerchr2:17026774..17035709hg19UCSC Ensembl
Outerchr2:17023752..17037320hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3813569
hg1913569
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv165n97
Supporting Variantsnssv4007597
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155190
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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