A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3554903



Internal ID18409293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:82395993..82396465hg38UCSC Ensembl
Outerchr17:82395969..82396584hg38UCSC Ensembl
Innerchr17:80353869..80354341hg19UCSC Ensembl
Outerchr17:80353845..80354460hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9753650
Samples
Known GenesOGFOD3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3554903
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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