A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114623



Internal ID21297889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:84999609..85011789hg38UCSC Ensembl
Innerchr8:85911844..85924024hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3812181
hg1912181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14085872
Samplessample40
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114623
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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