A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007647



Internal ID7072742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:70254460..70266566hg38UCSC Ensembl
Outerchr15:70546799..70558905hg19UCSC Ensembl
Outerchr15:68333853..68345959hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3812107
hg1912107
hg1812107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565078
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007647
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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