A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1000455



Internal ID1859014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:8086710..8096933hg19UCSC Ensembl
Outerchr10:8126716..8136939hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg193971
hg183971
Variant TypeCNV Deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv3564858
SamplesHuRef
Known GenesFLJ45983, GATA3
Method
Analysis
PlatformSanger Sequencing + Illumina Human1Mv1 BeadChip + Agilent Custom 244K CGH Array + Affymetrix Genome-Wide Human SNP 6.0 Array + NimbleGen 42M CGH Array + Agilent Custom 24M CGH Array
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1000455
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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