A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091091



Internal ID22000324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84736060..84736060hg38UCSC Ensembl
chr16:84769666..84769666hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622370
Samples
Known GenesUSP10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091091
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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