A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18015928



Internal ID20582968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103606424..103612346hg38UCSC Ensembl
chr14:104072761..104078683hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg385923
hg195923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500231
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18015928
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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