A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197665



Internal ID20764705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16118764..16119055hg38UCSC Ensembl
chr19:16229574..16229865hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521435
Supporting Variants
Samples
Known GenesRAB8A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197665
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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