A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765160



Internal ID20541020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9309517..9309517hg38UCSC Ensembl
chr11:9331064..9331064hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288316
Samples
Known GenesTMEM41B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765160
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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