A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254040



Internal ID20821080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33441659..33442920hg38UCSC Ensembl
chr21:34813966..34815227hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg381262
hg191262
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598770
Supporting Variants
Samples
Known GenesTMEM50B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254040
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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