A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108213



Internal ID21275115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:36020781..36078760hg38UCSC Ensembl
Innerchr3:36062273..36120252hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3857980
hg1957980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110963
Supporting Variants
Samplessample217
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108213
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