A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3554694



Internal ID18755770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68231418..68231628hg38UCSC Ensembl
Outerchr17:68231380..68231676hg38UCSC Ensembl
Innerchr17:66227559..66227769hg19UCSC Ensembl
Outerchr17:66227521..66227817hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9753441
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3554694
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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