A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3552827



Internal ID18407217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89516520..89518523hg38UCSC Ensembl
Outerchr15:89516126..89518554hg38UCSC Ensembl
Innerchr15:90059751..90061754hg19UCSC Ensembl
Outerchr15:90059357..90061785hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382429
hg192429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9751574
Samples
Known GenesLINC00928
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3552827
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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