A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485312



Internal ID262704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20742160..20755545hg38UCSC Ensembl
chr10:21031089..21044474hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3813386
hg1913386
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031731
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485312
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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