A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958911



Internal ID22733968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63895321..63928331hg38UCSC Ensembl
chr20:62526674..62559684hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3833011
hg1933011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390270
Samples
Known GenesDNAJC5, MIR941-1, MIR941-2, MIR941-3, MIR941-4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958911
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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