A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3554684



Internal ID18409074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67731280..67731509hg38UCSC Ensembl
Outerchr17:67731226..67731541hg38UCSC Ensembl
Innerchr17:65727396..65727625hg19UCSC Ensembl
Outerchr17:65727342..65727657hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9753431
Samples
Known GenesNOL11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3554684
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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