A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564798



Internal ID7035898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:124729380..124738866hg38UCSC Ensembl
Outerchr10:126417949..126427435hg19UCSC Ensembl
Outerchr10:126407939..126417425hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg389487
hg199487
hg189487
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1000820
Supporting Variants
SamplesHuRef
Known GenesFAM53B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564798
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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