A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5494652



Internal ID271789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:58372737..58386517hg38UCSC Ensembl
chr13:58946871..58960651hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3813781
hg1913781
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17688158
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5494652
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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