A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18040100



Internal ID20607140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38845806..38918365hg38UCSC Ensembl
chr18:36425770..36498329hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3872560
hg1972560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519384
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18040100
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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