A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485667



Internal ID263051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80260597..80272269hg38UCSC Ensembl
chr8:81172832..81184504hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3811673
hg1911673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735829
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485667
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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