A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486409



Internal ID263776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20967567..20983434hg38UCSC Ensembl
chr10:21256496..21272363hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3815868
hg1915868
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031753
Samples
Known GenesNEBL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486409
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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