A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644553



Internal ID21836600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63794205..63804635hg38UCSC Ensembl
chr20:62425558..62435988hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3810431
hg1910431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6060014
Supporting Variants
Samples
Known GenesZBTB46
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644553
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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