A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012076



Internal ID21921419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79745427..79852416hg38UCSC Ensembl
chr10:81505183..81612172hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38106990
hg19106990
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581135
Samples
Known GenesLOC642361
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012076
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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