A curated catalogue of human genomic structural variation




Variant Details

Variant: esv996549



Internal ID6732493
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3566384
SamplesHuRef
Known GenesCCDC15
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv996549
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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