A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009806



Internal ID7074100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:67112126..67113494hg38UCSC Ensembl
Outerchr15:67404464..67405832hg19UCSC Ensembl
Outerchr15:65191518..65192886hg18UCSC Ensembl
Cytoband15q22.33
Allele length
AssemblyAllele length
hg381369
hg191369
hg181369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563913
SamplesHuRef
Known GenesSMAD3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009806
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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