A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080997



Internal ID21990230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65609333..65609333hg38UCSC Ensembl
chr11:65376804..65376804hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581720
Samples
Known GenesMAP3K11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080997
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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