A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958498



Internal ID22733560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38783169..38783224hg38UCSC Ensembl
chr20:37411812..37411867hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397173
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958498
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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