A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081978



Internal ID21991211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6281166..6281166hg38UCSC Ensembl
chr10:6323129..6323129hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590039
Samples
Known GenesLOC399715
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081978
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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