A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020262



Internal ID21929605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92705151..92763194hg38UCSC Ensembl
chr10:94464908..94522951hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3858044
hg1958044
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586023
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020262
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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