A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517140



Internal ID20890501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45640898..45641375hg38UCSC Ensembl
chr19:46144156..46144633hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198892
Samples
Known GenesEML2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517140
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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