A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14455078



Internal ID22143471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87918874..88139672hg38UCSC Ensembl
chr9:90533789..90754587hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38220799
hg19220799
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3544782
Supporting Variants
SamplesHG00513
Known GenesCDK20, SPATA31C1, SPATA31C2
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14455078
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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