A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931965



Internal ID22707256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16241068..16241732hg38UCSC Ensembl
chr20:16221713..16222377hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38665
hg19665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402110
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931965
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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