A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490524



Internal ID267777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:12858608..12858898hg38UCSC Ensembl
chr8:12716117..12716407hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17007428
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490524
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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