A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18112359



Internal ID20679399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17342560..17342926hg38UCSC Ensembl
chr4:17344183..17344549hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367585
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18112359
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00058


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