A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476774



Internal ID254377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28639235..28643642hg38UCSC Ensembl
chr8:28496752..28501159hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg384408
hg194408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17011103
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476774
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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