A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1000739



Internal ID26442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6022806..6022878hg38UCSC Ensembl
chr10:6064769..6064841hg19UCSC Ensembl
chr10:6104775..6104847hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3873
hg1973
hg1873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3584858
SamplesHuRef
Known GenesIL2RA
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1000739
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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