A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920245



Internal ID22695468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8251254..8254142hg38UCSC Ensembl
chr11:8272801..8275689hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382889
hg192889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354830
Samples
Known GenesLMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920245
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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