A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236684



Internal ID20803724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9749393..9750123hg38UCSC Ensembl
chr11:9770940..9771670hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587823
Supporting Variants
Samples
Known GenesSWAP70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236684
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