A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487635



Internal ID264968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33564039..33577467hg38UCSC Ensembl
chr10:33852967..33866395hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3813429
hg1913429
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031471
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487635
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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