A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113176



Internal ID21296442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68508914..68515499hg38UCSC Ensembl
Innerchr17:66505055..66511640hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg386586
hg196586
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098576
Samplessample360
Known GenesPRKAR1A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113176
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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