A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599958



Internal ID20973029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36620432..36620581hg38UCSC Ensembl
chr20:35248835..35248984hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252553
Samples
Known GenesSLA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599958
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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