A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199096



Internal ID20766136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9501509..9505915hg38UCSC Ensembl
chr19:9612185..9616591hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384407
hg194407
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535230
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199096
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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