A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920914



Internal ID22696137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64818651..64822332hg38UCSC Ensembl
chr11:64586123..64589804hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg383682
hg193682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv268n209
Supporting Variantsnssv17355536
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920914
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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