A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17399458



Internal ID22457328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51895831..51901732hg38UCSC Ensembl
chr20:50512370..50518271hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg385902
hg195902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5953802
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17399458
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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