A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488554



Internal ID265862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58052774..58053084hg38UCSC Ensembl
chr8:58965333..58965643hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17012404
Samples
Known GenesFAM110B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488554
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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