A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218579



Internal ID22363875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13196115..13196397hg38UCSC Ensembl
chr16:13289972..13290254hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14375932, nssv14383371
SamplesNA19238, NA19239
Known GenesSHISA9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218579
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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