A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116713



Internal ID21299979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:113441714..113446657hg38UCSC Ensembl
Innerchr8:114453943..114458886hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg384944
hg194944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088294
Samplessample400
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116713
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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