A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18040141



Internal ID20607181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39282748..39462509hg38UCSC Ensembl
chr18:36862712..37042473hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38179762
hg19179762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519842
Supporting Variants
Samples
Known GenesLINC00669
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18040141
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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