A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599752



Internal ID20972823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37313139..37313874hg38UCSC Ensembl
chr21:38685441..38686176hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38736
hg19736
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254722
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599752
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer