A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254698



Internal ID20821738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36255330..36256277hg38UCSC Ensembl
chr21:37627628..37628575hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38948
hg19948
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596300
Supporting Variants
Samples
Known GenesDOPEY2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254698
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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