A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121064



Internal ID20688104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:79611117..79611633hg38UCSC Ensembl
chr4:80532271..80532787hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376271
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121064
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00097


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