A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121282



Internal ID20688322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98716438..98716940hg38UCSC Ensembl
chr4:99637589..99638091hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6378307
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121282
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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