A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114152



Internal ID21297418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:90599679..90941421hg38UCSC Ensembl
Innerchr5:89895496..90237238hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38341743
hg19341743
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14109365
Samplessample322
Known GenesGPR98
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114152
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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