A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099366



Internal ID21272534
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 StatusS
Merged Variantsnsv3116644
Supporting Variants
Samplessample179
Known GenesMIR8078, ROCK1P1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099366
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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