A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17627064



Internal ID21819111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33502894..33503018hg38UCSC Ensembl
chr20:32090700..32090824hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6055014
Supporting Variants
Samples
Known GenesCBFA2T2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17627064
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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