A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596293



Internal ID20969364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17618584..17619486hg38UCSC Ensembl
chr21:18990902..18991804hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38903
hg19903
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596293
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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