A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113329



Internal ID21296595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:41572156..41630783hg38UCSC Ensembl
Innerchr5:41572258..41630885hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3858628
hg1958628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14109316
Samplessample307
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113329
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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