A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189447



Internal ID20756487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:2873583..2876495hg38UCSC Ensembl
chr18:2873581..2876493hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg382913
hg192913
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533826
Supporting Variants
Samples
Known GenesEMILIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189447
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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