A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477045



Internal ID254640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92231873..92257319hg38UCSC Ensembl
chr8:93244101..93269547hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3825447
hg1925447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17015628
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477045
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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