A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082052



Internal ID21991285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69332390..69332390hg38UCSC Ensembl
chr10:71092146..71092146hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587625
Samples
Known GenesHK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082052
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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