A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198945



Internal ID20765985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47318326..47342377hg38UCSC Ensembl
chr19:47821583..47845634hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3824052
hg1924052
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521580
Supporting Variants
Samples
Known GenesC5AR1, C5AR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198945
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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