A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198268



Internal ID20765308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50018966..50089286hg38UCSC Ensembl
chr19:50522223..50592543hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3870321
hg1970321
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516773
Supporting Variants
Samples
Known GenesFLJ26850, VRK3, ZNF473
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198268
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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