A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9753353



Internal ID18380913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:59067745..59067848hg38UCSC Ensembl
Outerchr17:59067736..59067858hg38UCSC Ensembl
Innerchr17:57145106..57145209hg19UCSC Ensembl
Outerchr17:57145097..57145219hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3554606
Supporting Variants
Samples
Known GenesTRIM37
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9753353
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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