A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559820



Internal ID332843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49648131..49648271hg38UCSC Ensembl
chr13:50222267..50222407hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17687657
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559820
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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