A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925135



Internal ID22700362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62325417..62389619hg38UCSC Ensembl
chr11:62092889..62157091hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3864203
hg1964203
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364674
Samples
Known GenesASRGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925135
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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