A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924568



Internal ID22699795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62388564..62397557hg38UCSC Ensembl
chr11:62156036..62165029hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg388994
hg198994
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353113
Samples
Known GenesASRGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924568
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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