A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5952787



Internal ID22728091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63861059..63861108hg38UCSC Ensembl
chr20:62492412..62492461hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389979
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5952787
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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