A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198329



Internal ID20765369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52319886..52344851hg38UCSC Ensembl
chr19:52823139..52848104hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3824966
hg1924966
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530599
Supporting Variants
Samples
Known GenesZNF480, ZNF610
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198329
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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