A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990884



Internal ID7077015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:109810921..109818976hg38UCSC Ensembl
Outerchr10:111570679..111578734hg19UCSC Ensembl
Outerchr10:111560669..111568724hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg388056
hg198056
hg188056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv16e180
Supporting Variantsessv3563853
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990884
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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