A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3566384



Internal ID6691080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124960250..124960357hg38UCSC Ensembl
chr11:124830146..124830253hg19UCSC Ensembl
chr11:124335356..124335463hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38108
hg19108
hg18108
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv996549
Supporting Variants
SamplesHuRef
Known GenesCCDC15
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3566384
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