A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998825



Internal ID7064578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125091518..125092472hg38UCSC Ensembl
chr10:126780087..126781041hg19UCSC Ensembl
chr10:126770077..126771031hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38955
hg19955
hg18955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3582779
SamplesHuRef
Known GenesCTBP2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998825
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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