A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18040377



Internal ID20607417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23676075..23684804hg38UCSC Ensembl
chr18:21256039..21264768hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg388730
hg198730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535259
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18040377
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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