A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254194



Internal ID20821234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:19130360..23504699hg38UCSC Ensembl
chr21:20502678..24877018hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg384374340
hg194374341
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599226
Supporting Variants
Samples
Known GenesD21S2088E, LINC00308, LINC00317, LINC00320, NCAM2, RNU6-67P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254194
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00013


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