A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086336



Internal ID21995569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9309520..9309520hg38UCSC Ensembl
chr11:9331067..9331067hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593678
Samples
Known GenesTMEM41B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086336
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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