A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7534396



Internal ID10465992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:6055413..6055911hg38UCSC Ensembl
Outerchr10:6097376..6097874hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38499
hg19499
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3264829
Supporting Variants
SamplesHuRef
Known GenesIL2RA
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7534396
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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