A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558891



Internal ID331943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34191720..34251451hg38UCSC Ensembl
chr3:34233212..34292943hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3859732
hg1959732
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16931488
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558891
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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