A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751645



Internal ID18725891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:97410095..97410367hg38UCSC Ensembl
Outerchr15:97410072..97410411hg38UCSC Ensembl
Innerchr15:97953325..97953597hg19UCSC Ensembl
Outerchr15:97953302..97953641hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552898
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751645
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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