A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518154



Internal ID20891515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48929779..48936959hg38UCSC Ensembl
chr19:49433036..49440216hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg387181
hg197181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047102
Samples
Known GenesDHDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518154
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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