A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4115028



Internal ID11397567
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1104397
Supporting Variants
SamplesHuRef
Known GenesSIRT3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4115028
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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