A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5474444



Internal ID252103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85045450..85058624hg38UCSC Ensembl
chr8:85957685..85970859hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3813175
hg1913175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17015452
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5474444
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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