A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559764



Internal ID332787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31370203..31370218hg38UCSC Ensembl
chr19:31861109..31861124hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3816
hg1916
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722757
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559764
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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