A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192240



Internal ID20759280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:60008001..60024300hg38UCSC Ensembl
chr18:57675233..57691532hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3816300
hg1916300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528993
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192240
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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