A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565371



Internal ID7036753
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv997298
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565371
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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