A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18040491



Internal ID20607531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38106162..38106530hg38UCSC Ensembl
chr18:35686126..35686494hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523841
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18040491
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00043


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