A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009453



Internal ID21918796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78092640..78094479hg38UCSC Ensembl
chr10:79852397..79854236hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381840
hg191840
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590855
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009453
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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