A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9745896



Internal ID18720142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133291307..133292331hg38UCSC Ensembl
Outerchr10:133291202..133292532hg38UCSC Ensembl
Innerchr10:135104811..135105835hg19UCSC Ensembl
Outerchr10:135104706..135106036hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381331
hg191331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3547149
Supporting Variants
Samples
Known GenesTUBGCP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9745896
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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