A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517268



Internal ID20890629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2200079..2233054hg38UCSC Ensembl
chr19:2200078..2233053hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3832976
hg1932976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198497
Samples
Known GenesDOT1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517268
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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