A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254709



Internal ID20821749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36388488..36389594hg38UCSC Ensembl
chr21:37760786..37761892hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg381107
hg191107
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596104
Supporting Variants
Samples
Known GenesCHAF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254709
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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