A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990393



Internal ID7061519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100511533..100511971hg38UCSC Ensembl
chr15:101051738..101052176hg19UCSC Ensembl
chr15:98869261..98869699hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38439
hg19439
hg18439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3584966
SamplesHuRef
Known GenesCERS3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990393
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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