A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5494876



Internal ID272005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26184328..26187057hg38UCSC Ensembl
chr13:26758465..26761194hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg382730
hg192730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5494876
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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