A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751674



Internal ID18725920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99031286..99032203hg38UCSC Ensembl
Outerchr15:99031253..99032435hg38UCSC Ensembl
Innerchr15:99574515..99575432hg19UCSC Ensembl
Outerchr15:99574482..99575664hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381183
hg191183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552927
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751674
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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