A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492746



Internal ID269950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81884347..81907235hg38UCSC Ensembl
chr8:82796582..82819470hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3822889
hg1922889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17013955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492746
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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