A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253997



Internal ID20821037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31721846..31722713hg38UCSC Ensembl
chr21:33094159..33095026hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38868
hg19868
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596452
Supporting Variants
Samples
Known GenesSCAF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253997
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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