A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4361831



Internal ID11297683
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1206079
Supporting Variants
SamplesHuRef
Known GenesALDH3B2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4361831
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer