A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18019559



Internal ID20586599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:56364201..56368100hg38UCSC Ensembl
chr14:56830919..56834818hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484897
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18019559
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001


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