A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14372957



Internal ID22138760
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3238382
Supporting Variants
SamplesHG00513
Known GenesCTRB1, CTRB2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14372957
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