A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170092



Internal ID21314153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23813525..23935968hg38UCSC Ensembl
Outerchr16:23811667..23938591hg38UCSC Ensembl
Innerchr16:23824846..23947289hg19UCSC Ensembl
Outerchr16:23822988..23949912hg19UCSC Ensembl
Innerchr16:23732347..23854790hg18UCSC Ensembl
Outerchr16:23730489..23857413hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38126925
hg19126925
hg18126925
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14246165, nssv14252237
SamplesPML_1, PML_2
Known GenesPRKCB
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170092
Frequency
Sample Size93
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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