A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1049168



Internal ID5179275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121584763..121584879hg38UCSC Ensembl
chr10:123344277..123344393hg19UCSC Ensembl
chr10:123334267..123334383hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38117
hg19117
hg18117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4319856
SamplesHuRef
Known GenesFGFR2
MethodSequencing
Analysis
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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