A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116527



Internal ID21402980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33536230..33536357hg38UCSC Ensembl
chr20:32124036..32124163hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600320
Supporting Variants
SamplesHG00171
Known GenesCBFA2T2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116527
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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