A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563582



Internal ID7036342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:45404931..45415083hg38UCSC Ensembl
Outerchr11:45426481..45436633hg19UCSC Ensembl
Outerchr11:45383057..45393209hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3810153
hg1910153
hg1810153
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv996050
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563582
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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