A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112963



Internal ID21296229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76492549..76496972hg38UCSC Ensembl
Innerchr18:74204505..74208929hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg384424
hg194425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100023
Samplessample197
Known GenesFLJ44313, ZNF516
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112963
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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