A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744242



Internal ID18718488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128794530..128795492hg38UCSC Ensembl
Outerchr9:128794469..128795607hg38UCSC Ensembl
Innerchr9:131556809..131557771hg19UCSC Ensembl
Outerchr9:131556748..131557886hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381139
hg191139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545495
Supporting Variants
Samples
Known GenesTBC1D13
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744242
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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