A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598283



Internal ID20971354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33502651..33503025hg38UCSC Ensembl
chr20:32090457..32090831hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251772
Samples
Known GenesCBFA2T2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598283
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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