A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915868



Internal ID22691086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121478926..121478981hg38UCSC Ensembl
chr11:121349635..121349690hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359672
Samples
Known GenesSORL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915868
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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