A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18163786



Internal ID20730826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:117590204..117628701hg38UCSC Ensembl
chr8:118602443..118640940hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg3838498
hg1938498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418420
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18163786
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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