A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751156



Internal ID18725402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:47428445..47428607hg38UCSC Ensembl
Outerchr15:47428415..47428612hg38UCSC Ensembl
Innerchr15:47720642..47720804hg19UCSC Ensembl
Outerchr15:47720612..47720809hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552409
Supporting Variants
Samples
Known GenesSEMA6D
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751156
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