A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121474



Internal ID20688514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97123778..97124251hg38UCSC Ensembl
chr4:98044929..98045402hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6389910
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121474
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00266


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