A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085658



Internal ID21994891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102364173..102364173hg38UCSC Ensembl
chr11:102234904..102234904hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596193
Samples
Known GenesBIRC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085658
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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