A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115224



Internal ID21298490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56115986..56123450hg38UCSC Ensembl
Innerchr19:56627355..56634819hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg387465
hg197465
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101365
Samplessample306
Known GenesZNF787
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115224
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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