A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3582779



Internal ID7054161
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 StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv998825
Supporting Variants
SamplesHuRef
Known GenesCTBP2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3582779
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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