A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083802



Internal ID21285961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:20072182..20200533hg38UCSC Ensembl
Innerchr6:20072413..20200764hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38128352
hg19128352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113273
Supporting Variants
Samplessample381
Known GenesMBOAT1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083802
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