A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914833



Internal ID22690050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57776396..57777043hg38UCSC Ensembl
chr11:57543868..57544515hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38648
hg19648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363299
Samples
Known GenesCTNND1, TMX2-CTNND1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914833
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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