A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098670



Internal ID21287114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68288629..68294354hg38UCSC Ensembl
Innerchr17:66284770..66290495hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg385726
hg195726
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116175
Supporting Variants
Samplessample397
Known GenesARSG, SLC16A6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098670
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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