A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217565



Internal ID20784605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21477605..21478365hg38UCSC Ensembl
chr10:21766534..21767294hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38761
hg19761
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589053
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217565
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