A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14453705



Internal ID22143351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63252862..63392265hg38UCSC Ensembl
chr9:67207835..67347237hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38139404
hg19139403
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3552360
Supporting Variants
SamplesHG00513
Known GenesAQP7P1
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14453705
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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