A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203289



Internal ID20770329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33517560..33518059hg38UCSC Ensembl
chr20:32105366..32105865hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519264
Supporting Variants
Samples
Known GenesCBFA2T2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203289
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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