A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226968



Internal ID22369598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22844980..22845477hg38UCSC Ensembl
chr16:22856301..22856798hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14390593, nssv14385966, nssv14387709
SamplesNA19238, NA19239, NA19240
Known GenesHS3ST2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226968
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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