A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081587



Internal ID21990820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102553939..102553939hg38UCSC Ensembl
chr10:104313696..104313696hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg382565
hg192565
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586679
Samples
Known GenesSUFU
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081587
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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