A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733234



Internal ID20509162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23150073..23158251hg38UCSC Ensembl
chr20:23130710..23138888hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg388179
hg198179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282540
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733234
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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