A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928206



Internal ID22703442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4984283..4984866hg38UCSC Ensembl
chr20:4964929..4965512hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38584
hg19584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393774
Samples
Known GenesSLC23A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928206
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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