A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3261718



Internal ID11281384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:87516040..87516811hg38UCSC Ensembl
Outerchr10:89275797..89276568hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38772
hg19772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7531285
SamplesHuRef
Known GenesMINPP1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3261718
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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