A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085106



Internal ID21994339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85914796..85914796hg38UCSC Ensembl
chr16:85948402..85948402hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619664
Samples
Known GenesIRF8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085106
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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