A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155972



Internal ID22086477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:74099008..74102720hg38UCSC Ensembl
Outerchr3:74097816..74106513hg38UCSC Ensembl
Innerchr3:74148159..74151871hg19UCSC Ensembl
Outerchr3:74146967..74155664hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg388698
hg198698
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016405
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155972
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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