A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3238382



Internal ID22374134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75205515..75223451hg38UCSC Ensembl
chr16:75239413..75257349hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3817937
hg1917937
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14372957, nssv14392038, nssv14384853, nssv14391356, nssv14386578, nssv14379998, nssv14378324, nssv14379203, nssv14385365
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesCTRB1, CTRB2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3238382
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer