A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052507



Internal ID21961740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32111096..32111535hg38UCSC Ensembl
chr20:30698899..30699338hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636358
Samples
Known GenesTM9SF4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052507
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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