A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252586



Internal ID20819626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49933118..49934654hg38UCSC Ensembl
chr20:48549655..48551191hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg381537
hg191537
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599991
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252586
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00156


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