A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525971



Internal ID302118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32434189..32434397hg38UCSC Ensembl
chr19:32925095..32925303hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722817
Samples
Known GenesDPY19L3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525971
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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