A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116354



Internal ID21299620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:44847003..44873259hg38UCSC Ensembl
Innerchr2:45074142..45100398hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3826257
hg1926257
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102515
Samplessample61
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116354
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer