A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3552360



Internal ID22421254
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14453683, nssv14460320, nssv14455245, nssv14453705, nssv14466556, nssv14460014, nssv14458251, nssv14453023, nssv14459810
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesAQP7P1
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3552360
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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