A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528161



Internal ID22397546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14843251..14843774hg38UCSC Ensembl
chr12:14996185..14996708hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14360380, nssv14360379
SamplesNA19238, NA19240
Known GenesART4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528161
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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