A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5508582



Internal ID285269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124446844..124446898hg38UCSC Ensembl
chr10:126135413..126135467hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038836
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5508582
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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