A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518321



Internal ID20891682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48924480..48943962hg38UCSC Ensembl
chr19:49427737..49447219hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3819483
hg1919483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047100
Samples
Known GenesDHDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518321
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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