A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950475



Internal ID22725875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51302001..51302074hg38UCSC Ensembl
chr20:49918538..49918611hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950475
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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