A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17405704



Internal ID22463574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:23943621..24435118hg38UCSC Ensembl
chr21:25315936..25807432hg19UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg38491498
hg19491497
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971326
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17405704
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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