A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112214



Internal ID21295480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:31815254..31852924hg38UCSC Ensembl
Innerchr19:32306160..32343830hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3837671
hg1937671
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101102
Samplessample40
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112214
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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