A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067448



Internal ID20634488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33554638..33559776hg38UCSC Ensembl
chr20:32142444..32147582hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg385139
hg195139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526471
Supporting Variants
Samples
Known GenesCBFA2T2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067448
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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