A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198891



Internal ID20765931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45635201..45661500hg38UCSC Ensembl
chr19:46138459..46164758hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3826300
hg1926300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534174
Supporting Variants
Samples
Known GenesC19orf83, EML2, MIR330
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198891
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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