A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29946



Internal ID11047469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38275639..38312843hg38UCSC Ensembl
Innerchr7:38315240..38352444hg19UCSC Ensembl
Innerchr7:38281765..38318969hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3837205
hg1937205
hg1837205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84185
SamplesWATSON
Known Genes
MethodOligo aCGH
AnalysisThe data were analyzed using the CGH Analytics software.
PlatformAgilent-014584 Human Genome 244K CGH Microarray (Alpha Test)
Comments
ReferenceWheeler_et_al_2008
Pubmed ID18421352
Accession Number(s)esv29946
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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