A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3554442



Internal ID22423303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105053366..105056276hg38UCSC Ensembl
chr9:107815647..107818557hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg382911
hg192911
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14453130, nssv14461079, nssv14464633, nssv14466985, nssv14459485, nssv14464584, nssv14454043, nssv14458468, nssv14459110
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3554442
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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