A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081134



Internal ID21990367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67782843..67782843hg38UCSC Ensembl
chr16:67816746..67816746hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622421
Samples
Known GenesRANBP10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081134
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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