A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112722



Internal ID21295988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:54927992..54931841hg38UCSC Ensembl
Innerchr18:52595223..52599072hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg383850
hg193850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv528n145
Supporting Variantsnssv14099558
Samplessample111
Known GenesCCDC68
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112722
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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