A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1008549



Internal ID7073526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:70246549..70252571hg38UCSC Ensembl
Outerchr11:70092655..70098677hg19UCSC Ensembl
Outerchr11:69770303..69776325hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg386023
hg196023
hg186023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565652
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1008549
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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