A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18022900



Internal ID20589940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93688505..93689130hg38UCSC Ensembl
chr14:94154851..94155476hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513743
Supporting Variants
Samples
Known GenesUNC79
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18022900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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