A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476889



Internal ID254487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73090958..73109145hg38UCSC Ensembl
chr8:74003193..74021380hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3818188
hg1918188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17012053
Samples
Known GenesSBSPON
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476889
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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