A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099397



Internal ID21275955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:54928190..54931841hg38UCSC Ensembl
Innerchr18:52595421..52599072hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg383652
hg193652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117270
Supporting Variants
Samplessample23
Known GenesCCDC68
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099397
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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