A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199707



Internal ID20766747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57477116..57491703hg38UCSC Ensembl
chr19:57988484..58003071hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3814588
hg1914588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518990
Supporting Variants
Samples
Known GenesZNF419, ZNF772
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199707
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00161


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