A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112347



Internal ID21295613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57515067..57519036hg38UCSC Ensembl
Innerchr15:57807265..57811234hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg383970
hg193970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097233
Samplessample380
Known GenesCGNL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112347
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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