A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483489



Internal ID260925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74497913..74498025hg38UCSC Ensembl
chr8:75410148..75410260hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17012170
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483489
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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