A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083790



Internal ID21285684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10481673..10698466hg38UCSC Ensembl
Innerchr6:10481906..10698699hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38216794
hg19216794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113907
Supporting Variants
Samplessample379
Known GenesC6orf52, GCNT2, PAK1IP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083790
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