A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997298



Internal ID7081268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:44710588..44714248hg38UCSC Ensembl
Outerchr11:44732138..44735798hg19UCSC Ensembl
Outerchr11:44688714..44692374hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg383661
hg193661
hg183661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565371
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997298
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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