A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116644



Internal ID21299910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69616..146710hg38UCSC Ensembl
Innerchr18:69616..146710hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3877095
hg1977095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099454, nssv14099408, nssv14100203, nssv14099443, nssv14099348, nssv14099366
Samplessample179, sample52, sample312, sample28, sample48, sample169
Known GenesMIR8078, ROCK1P1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116644
Frequency
Sample Size467
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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