A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251803



Internal ID20818843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34040019..34040122hg38UCSC Ensembl
chr20:32627825..32627928hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596200
Supporting Variants
Samples
Known GenesRALY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251803
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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