A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476529



Internal ID254136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:1799303..1799409hg38UCSC Ensembl
chr8:1747469..1747575hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17005548
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476529
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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