A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098628



Internal ID21285630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68288629..68294374hg38UCSC Ensembl
Innerchr17:66284770..66290515hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg385746
hg195746
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110515
Supporting Variants
Samplessample378
Known GenesARSG, SLC16A6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098628
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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