A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561842



Internal ID334810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:19275969..19277011hg38UCSC Ensembl
chr21:20648286..20649328hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381043
hg191043
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17734239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561842
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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