A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3552592



Internal ID18753668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:66585386..66586049hg38UCSC Ensembl
Outerchr15:66585288..66586172hg38UCSC Ensembl
Innerchr15:66877724..66878387hg19UCSC Ensembl
Outerchr15:66877626..66878510hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38885
hg19885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9751339
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3552592
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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