A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1011225



Internal ID7059987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:15187920..15197806hg38UCSC Ensembl
Outerchr6:15188151..15198037hg19UCSC Ensembl
Outerchr6:15296130..15306016hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg389887
hg199887
hg189887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565617
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1011225
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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