A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1206079



Internal ID12022516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67669335..67669687hg38UCSC Ensembl
chr11:67436806..67437158hg19UCSC Ensembl
chr11:67193382..67193734hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38353
hg19353
hg18353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4361831
SamplesHuRef
Known GenesALDH3B2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1206079
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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