A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112437



Internal ID21295703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68289411..68294374hg38UCSC Ensembl
Innerchr17:66285552..66290515hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg384964
hg194964
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv506n145
Supporting Variantsnssv14098611
Samplessample372
Known GenesARSG, SLC16A6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112437
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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