A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562534



Internal ID335486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31820112..31841293hg38UCSC Ensembl
chr13:32394249..32415430hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3821182
hg1921182
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686682
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562534
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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