A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486976



Internal ID264326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80809370..80815127hg38UCSC Ensembl
chr10:82569126..82574883hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg385758
hg195758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038682
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486976
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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