A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18042091



Internal ID20609131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48785508..48789372hg38UCSC Ensembl
chr18:46311879..46315743hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg383865
hg193865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528899
Supporting Variants
Samples
Known GenesCTIF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18042091
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00082


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