A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086402



Internal ID21269371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:117905029..117909852hg38UCSC Ensembl
Innerchr6:118226192..118231015hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg384824
hg194824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113676
Supporting Variants
Samplessample138
Known GenesSLC35F1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086402
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