A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111024



Internal ID21294290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:93139443..93142869hg38UCSC Ensembl
Innerchr5:92475149..92478575hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg383427
hg193427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096702
Samplessample13
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111024
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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