A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14456429



Internal ID22269715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40691369..40868523hg38UCSC Ensembl
chr9:66664196..66821551hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38177155
hg19157356
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3546223
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14456429
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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