A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18040149



Internal ID20607189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39359353..39455471hg38UCSC Ensembl
chr18:36939317..37035435hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3896119
hg1996119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525651
Supporting Variants
Samples
Known GenesLINC00669
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18040149
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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