A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226077



Internal ID22369008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58750659..58750792hg38UCSC Ensembl
chr15:59042858..59042991hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14384990, nssv14378916
SamplesNA19238, NA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226077
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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