A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254678



Internal ID20821718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:34363514..34364486hg38UCSC Ensembl
chr21:35735813..35736785hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38973
hg19973
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599813
Supporting Variants
Samples
Known GenesKCNE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254678
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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