A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104829



Internal ID21272220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:196188143..196191840hg38UCSC Ensembl
Innerchr2:197052867..197056564hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg383698
hg193698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116733
Supporting Variants
Samplessample174
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104829
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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