A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5493493



Internal ID270668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34693423..34713917hg38UCSC Ensembl
chr8:34550941..34571435hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3820495
hg1920495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17011357
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5493493
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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