A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047829



Internal ID20614869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38943326..38960819hg38UCSC Ensembl
chr19:39433966..39451459hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3817494
hg1917494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533968
Supporting Variants
Samples
Known GenesFBXO17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047829
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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