A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924578



Internal ID22699805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111789707..111790064hg38UCSC Ensembl
chr11:111660431..111660788hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358614
Samples
Known GenesALG9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924578
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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