A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1109336



Internal ID11925774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131952234..131952298hg38UCSC Ensembl
chr10:133765738..133765802hg19UCSC Ensembl
chr10:133615728..133615792hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3865
hg1965
hg1865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3605993
SamplesHuRef
Known GenesPPP2R2D
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1109336
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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