A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191905



Internal ID20758945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13403264..13407309hg38UCSC Ensembl
chr18:13403263..13407308hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg384046
hg194046
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521842
Supporting Variants
Samples
Known GenesLDLRAD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191905
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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