A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990531



Internal ID7076662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119080165..119080353hg38UCSC Ensembl
chr10:120839677..120839865hg19UCSC Ensembl
chr10:120829667..120829855hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38189
hg19189
hg18189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3568070
SamplesHuRef
Known GenesEIF3A
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990531
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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