A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1049168



Internal ID1017106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123344277..123344393hg19UCSC Ensembl
chr10:123334267..123334383hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg19117
hg18117
Variant TypeCNV Deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv4319856
SamplesHuRef
Known GenesFGFR2
Method
AnalysisRegion identical to calls - DGVa curated
PlatformSanger Sequencing
Comments
ReferenceLevy et al 2007
Pubmed ID17803354
Accession Number(s)esv1049168
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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