A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5546596



Internal ID320529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41373621..41373621hg38UCSC Ensembl
chr19:41879526..41879526hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723493
Samples
Known GenesTMEM91
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5546596
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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