A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254082



Internal ID20821122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62183874..62186576hg38UCSC Ensembl
chr20:60758930..60761632hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382703
hg192703
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597987
Supporting Variants
Samples
Known GenesMTG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254082
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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