A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5475828



Internal ID253459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43349553..43357681hg38UCSC Ensembl
chr10:43845001..43853129hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg388129
hg198129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032752
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5475828
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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