A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043612



Internal ID20610652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69375682..69376136hg38UCSC Ensembl
chr18:67042918..67043372hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526576
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043612
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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