A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083879



Internal ID21287059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:143609239..143612316hg38UCSC Ensembl
Innerchr6:143930376..143933453hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg383078
hg193078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115931
Supporting Variants
Samplessample397
Known GenesPHACTR2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083879
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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