A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106231



Internal ID21282795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:183593723..184303116hg38UCSC Ensembl
Innerchr2:184458451..185167843hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38709394
hg19709393
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116223
Supporting Variants
Samplessample331
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106231
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