A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199376



Internal ID20766416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2880486..2894248hg38UCSC Ensembl
chr19:2880484..2894246hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3813763
hg1913763
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526382
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199376
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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