A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254349



Internal ID20821389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37211245..37211618hg38UCSC Ensembl
chr20:35839648..35840021hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598914
Supporting Variants
Samples
Known GenesRPN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254349
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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