A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745380



Internal ID20521388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33699073..33701313hg38UCSC Ensembl
chr20:32286879..32289119hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg382241
hg192241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291740
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745380
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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