A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086442



Internal ID21269932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169064281..169067088hg38UCSC Ensembl
Innerchr6:169464376..169467183hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382808
hg192808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111521
Supporting Variants
Samplessample145
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086442
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