A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199583



Internal ID20766623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4852984..4892241hg38UCSC Ensembl
chr19:4852996..4892253hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3839258
hg1939258
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529009
Supporting Variants
Samples
Known GenesARRDC5, PLIN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199583
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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