A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100244



Internal ID21283436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78794730..78808221hg38UCSC Ensembl
Innerchr18:76554730..76568221hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3813492
hg1913492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114321
Supporting Variants
Samplessample344
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100244
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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