A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116741



Internal ID21300007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:105528908..105683683hg38UCSC Ensembl
Innerchr2:106145365..106300140hg19UCSC Ensembl
Cytoband2q12.2
Allele length
AssemblyAllele length
hg38154776
hg19154776
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14106930
Samplessample403
Known GenesLOC285000
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116741
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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