A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253669



Internal ID20820709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:30707106..30707962hg38UCSC Ensembl
chr21:32079424..32080280hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38857
hg19857
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597210
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253669
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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