A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959481



Internal ID22734508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18980616..18986170hg38UCSC Ensembl
chr20:18961260..18966814hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg385555
hg195555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392321
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959481
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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