A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3584858



Internal ID6709554
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 StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1000739
Supporting Variants
SamplesHuRef
Known GenesIL2RA
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3584858
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer