A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096725



Internal ID21273304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:23505668..23656189hg38UCSC Ensembl
Innerchr5:23505777..23656298hg19UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg38150522
hg19150522
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114492
Supporting Variants
Samplessample19
Known GenesPRDM9
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096725
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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