A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14085104



Internal ID21272806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85572326..85628557hg38UCSC Ensembl
Innerchr7:85201642..85257873hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3856232
hg1956232
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115645
Supporting Variants
Samplessample182
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14085104
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