A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990417



Internal ID6726384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133015367..133015426hg38UCSC Ensembl
chr11:132885262..132885321hg19UCSC Ensembl
chr11:132390472..132390531hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3860
hg1960
hg1860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3585931
SamplesHuRef
Known GenesOPCML
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990417
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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