A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532498



Internal ID20905859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48942930..48945190hg38UCSC Ensembl
chr19:49446187..49448447hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg382261
hg192261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047106
Samples
Known GenesDHDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532498
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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