A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18019913



Internal ID20586953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:66399066..66399727hg38UCSC Ensembl
chr14:66865784..66866445hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6486289
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18019913
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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