A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623016



Internal ID21815063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2183934..2183934hg38UCSC Ensembl
chr19:2183933..2183933hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6104694
Supporting Variants
Samples
Known GenesDOT1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623016
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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