A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033654



Internal ID21942997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57723531..57733888hg38UCSC Ensembl
chr11:57491003..57501360hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3810358
hg1910358
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597317
Samples
Known GenesTMX2, TMX2-CTNND1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033654
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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