A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947618



Internal ID22723121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22665530..22683354hg38UCSC Ensembl
chr20:22646168..22663992hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3817825
hg1917825
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394802
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947618
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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