A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113759



Internal ID21297025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:7629863..7781370hg38UCSC Ensembl
Innerchr3:7671550..7823057hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38151508
hg19151508
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105959
Samplessample133
Known GenesGRM7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113759
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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