A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558751



Internal ID331807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40405456..40406277hg38UCSC Ensembl
chr19:40911363..40912184hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38822
hg19822
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723402
Samples
Known GenesPRX
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558751
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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