A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116274



Internal ID20683314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28095759..28104296hg38UCSC Ensembl
chr4:28097381..28105918hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg388538
hg198538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365755
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116274
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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