A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100299



Internal ID21286224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76489690..76494005hg38UCSC Ensembl
Innerchr18:74201646..74205961hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg384316
hg194316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112451
Supporting Variants
Samplessample385
Known GenesZNF516
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100299
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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