A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117393



Internal ID21300659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:56353766..56358794hg38UCSC Ensembl
Innerchr18:54020997..54026025hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg385029
hg195029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv529n145
Supporting Variantsnssv14100274
Samplessample370
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117393
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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