A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111732



Internal ID21294998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51492087..51495723hg38UCSC Ensembl
Innerchr19:51995341..51998977hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg383637
hg193637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101022
Samplessample14
Known GenesSIGLEC12
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111732
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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