A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933093



Internal ID22708401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7620221..7624354hg38UCSC Ensembl
chr20:7600868..7605001hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg384134
hg194134
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390645
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933093
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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