A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048833



Internal ID20615873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48677025..48697218hg38UCSC Ensembl
chr19:49180282..49200475hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3820194
hg1920194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517781
Supporting Variants
Samples
Known GenesFUT2, SEC1P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048833
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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