A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091658



Internal ID22000891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89290329..89290329hg38UCSC Ensembl
chr16:89356737..89356737hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634634
Samples
Known GenesANKRD11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091658
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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