A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14084860



Internal ID21289741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:43611849..43616491hg38UCSC Ensembl
Innerchr7:43651448..43656090hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg384643
hg194643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112659
Supporting Variants
Samplessample50
Known GenesSTK17A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14084860
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