A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214024



Internal ID22360792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25096623..25098002hg38UCSC Ensembl
chr15:25341770..25343149hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381380
hg191380
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14379262, nssv14375371
SamplesNA19239, NA19240
Known GenesSNORD116-25
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214024
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