A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086201



Internal ID21995434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96155509..96155509hg38UCSC Ensembl
chr11:95888673..95888673hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589506
Samples
Known GenesMAML2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086201
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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