A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909006



Internal ID22684216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105997150..105997304hg38UCSC Ensembl
chr11:105867877..105868031hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359387
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909006
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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