A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488477



Internal ID265789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41088897..41089319hg38UCSC Ensembl
chr8:40946416..40946838hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17009689
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488477
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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