A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598819



Internal ID20971890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41196245..41197390hg38UCSC Ensembl
chr21:42568172..42569317hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg381146
hg191146
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4604n223
Supporting Variantsnssv18254464
Samples
Known GenesBACE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598819
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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