A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112451



Internal ID21295717
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 StatusM
Merged Variants
Supporting Variantsnssv14100299, nssv14100014
Samplessample193, sample385
Known GenesZNF516
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112451
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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