A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3544782



Internal ID22413809
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14455078
SamplesHG00513
Known GenesCDK20, SPATA31C1, SPATA31C2
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3544782
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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