A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5505372



Internal ID282150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121889481..121899953hg38UCSC Ensembl
chr10:123648996..123659468hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3810473
hg1910473
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040363
Samples
Known GenesATE1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5505372
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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