A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5502152



Internal ID279028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20881562..20884011hg38UCSC Ensembl
chr13:21455701..21458150hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg382450
hg192450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17685983
Samples
Known GenesXPO4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5502152
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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