A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114242



Internal ID21297508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:55666132..55674948hg38UCSC Ensembl
Innerchr8:56578691..56587507hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg388817
hg198817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086210
Samplessample250
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114242
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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