A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1363864



Internal ID12180300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131952097..131952216hg38UCSC Ensembl
chr10:133765601..133765720hg19UCSC Ensembl
chr10:133615591..133615710hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38120
hg19120
hg18120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3739487
SamplesHuRef
Known GenesPPP2R2D
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1363864
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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