A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009681



Internal ID7059493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:47663540..47664377hg38UCSC Ensembl
Outerchr7:47703138..47703975hg19UCSC Ensembl
Outerchr7:47669663..47670500hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38838
hg19838
hg18838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564971
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009681
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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