A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597050



Internal ID20970121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17911287..17912305hg38UCSC Ensembl
chr21:19283604..19284622hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381019
hg191019
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254182
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597050
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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