A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914207



Internal ID22689424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134046061..134046150hg38UCSC Ensembl
chr11:133915956..133916045hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359001
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914207
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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