A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253371



Internal ID20820411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:55184625..55185629hg38UCSC Ensembl
chr20:53801164..53802168hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg381005
hg191005
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596774
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253371
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00038


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