A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751364



Internal ID18725610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68757243..68757556hg38UCSC Ensembl
Outerchr15:68757154..68757596hg38UCSC Ensembl
Innerchr15:69049582..69049895hg19UCSC Ensembl
Outerchr15:69049493..69049935hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552617
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751364
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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