A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081466



Internal ID21990699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32412717..32412717hg38UCSC Ensembl
chr11:32434263..32434263hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595704
Samples
Known GenesWT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081466
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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