A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529238



Internal ID22398631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51697177..51697290hg38UCSC Ensembl
chr15:51989374..51989487hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14381759
SamplesNA19238
Known GenesSCG3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529238
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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