A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14082905



Internal ID21281214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4774271..4779149hg38UCSC Ensembl
Innerchr6:4774505..4779383hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg384879
hg194879
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111282
Supporting Variants
Samplessample309
Known GenesCDYL
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14082905
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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