A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477410



Internal ID254993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106027657..106039033hg38UCSC Ensembl
chr8:107039885..107051261hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3811377
hg1911377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17015868
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477410
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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