A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476171



Internal ID253788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69946007..69952453hg38UCSC Ensembl
chr8:70858242..70864688hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg386447
hg196447
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17011997
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476171
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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