A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199590



Internal ID20766630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48602527..48617272hg38UCSC Ensembl
chr19:49105784..49120529hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3814746
hg1914746
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526815
Supporting Variants
Samples
Known GenesFAM83E, RPL18, SPACA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199590
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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