A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1011222



Internal ID7059984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:125939177..125944773hg38UCSC Ensembl
Outerchr11:125809072..125814668hg19UCSC Ensembl
Outerchr11:125314282..125319878hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg385597
hg195597
hg185597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565200
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1011222
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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