A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113495



Internal ID21296761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:104564337..104586538hg38UCSC Ensembl
Innerchr8:105576565..105598766hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3822202
hg1922202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087062
Samplessample107
Known GenesLRP12
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113495
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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