A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117197



Internal ID21300463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:73513037..73531987hg38UCSC Ensembl
Innerchr17:71509176..71528126hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3818951
hg1918951
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098845
Samplessample120
Known GenesSDK2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117197
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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