A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29949



Internal ID11047472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25282958..25337060hg38UCSC Ensembl
Innerchr1:25609449..25663551hg19UCSC Ensembl
Innerchr1:25482036..25536138hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3854103
hg1954103
hg1854103
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84188
SamplesWATSON
Known GenesRHD
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)esv29949
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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