A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5496228



Internal ID273307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97421214..97422200hg38UCSC Ensembl
chr13:98073468..98074454hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38987
hg19987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17694064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5496228
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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