A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964821



Internal ID22739756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22619448..22620838hg38UCSC Ensembl
chr20:22600086..22601476hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg381391
hg191391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399182
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5964821
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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