A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18112258



Internal ID20679298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15023293..15023774hg38UCSC Ensembl
chr4:15024917..15025398hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367419
Supporting Variants
Samples
Known GenesCPEB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18112258
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00168


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