A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115780



Internal ID21299046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:62436732..62492498hg38UCSC Ensembl
Innerchr8:63349291..63405057hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3855767
hg1955767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086146
Samplessample232
Known GenesNKAIN3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115780
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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