A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100023



Internal ID21273804
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 StatusS
Merged Variantsnsv3112963
Supporting Variants
Samplessample197
Known GenesFLJ44313, ZNF516
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100023
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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