A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492387



Internal ID269601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9501174..9504831hg38UCSC Ensembl
chr8:9358684..9362341hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg383658
hg193658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17008717
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492387
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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