A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595898



Internal ID20968969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29496994..29498684hg38UCSC Ensembl
chr21:30869314..30871004hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg381691
hg191691
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595898
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