A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155899



Internal ID22086404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:188714603..188742954hg38UCSC Ensembl
Outerchr2:188714283..188744525hg38UCSC Ensembl
Innerchr2:189579330..189607681hg19UCSC Ensembl
Outerchr2:189579010..189609252hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg3830243
hg1930243
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016130
Samples
Known GenesDIRC1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155899
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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