A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5531153



Internal ID307117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38897330..38897988hg38UCSC Ensembl
chr19:39387970..39388628hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723289
Samples
Known GenesSIRT2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5531153
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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