A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086059



Internal ID21995292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104244541..104244541hg38UCSC Ensembl
chr10:106004299..106004299hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086059
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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