A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112949



Internal ID21296215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:126970555..126975837hg38UCSC Ensembl
Innerchr8:127982800..127988082hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg385283
hg195283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14085786
Samplessample14
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112949
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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