A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498567



Internal ID275557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:54436502..54436585hg38UCSC Ensembl
chr13:55010637..55010720hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17687914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498567
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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