A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935755



Internal ID22711100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48929835..48936990hg38UCSC Ensembl
chr19:49433092..49440247hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg387156
hg197156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403225
Samples
Known GenesDHDH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935755
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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