A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598802



Internal ID20971873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1483705..1483769hg38UCSC Ensembl
chr20:1464350..1464414hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253548
Samples
Known GenesSIRPB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598802
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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