A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565356



Internal ID20938427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110265889..110395682hg38UCSC Ensembl
chr9:113028169..113157962hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38129794
hg19129794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279513
Samples
Known GenesSVEP1, TXNDC8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565356
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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