A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197389



Internal ID20764429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14030001..14032400hg38UCSC Ensembl
chr19:14140813..14143212hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516142
Supporting Variants
Samples
Known GenesIL27RA, RLN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197389
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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