A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215148



Internal ID22361576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83187222..83187318hg38UCSC Ensembl
chr15:83855974..83856070hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14385826, nssv14383086
SamplesNA19238, NA19240
Known GenesHDGFRP3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215148
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