A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1104397



Internal ID12267521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:223831..223975hg38UCSC Ensembl
chr11:223831..223975hg19UCSC Ensembl
chr11:213831..213975hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38145
hg19145
hg18145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4115028
SamplesHuRef
Known GenesSIRT3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1104397
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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