A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490515



Internal ID267769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:83573975..83583558hg38UCSC Ensembl
chr8:84486210..84495793hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg389584
hg199584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17014099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490515
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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