A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112430



Internal ID21295696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:88734760..88830567hg38UCSC Ensembl
Innerchr8:89746989..89842796hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3895808
hg1995808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14085918
Samplessample52
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112430
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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