A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5503991



Internal ID280802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32873927..32882423hg38UCSC Ensembl
chr13:33448065..33456561hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg388497
hg198497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686738
Samples
Known GenesLINC00423
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5503991
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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