A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909294



Internal ID22684504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110385687..110557735hg38UCSC Ensembl
chr11:110256411..110428459hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38172049
hg19172049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368909
Samples
Known GenesFDX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909294
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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