A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14467566



Internal ID22273045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60024806..60126538hg38UCSC Ensembl
chr17:58102167..58203899hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg38101733
hg19101733
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3557061
Supporting Variants
SamplesNA19239
Known GenesHEATR6, LOC645638, LOC653653, MIR4737
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14467566
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