A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117826



Internal ID21301092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:117590477..117593611hg38UCSC Ensembl
Innerchr8:118602716..118605850hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg383135
hg193135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14085337
Samplessample177
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117826
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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