A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2854902



Internal ID10874599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46581617..46585617hg38UCSC Ensembl
Innerchr10:46964000..46968000hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg384001
hg194001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7124469
SamplesHuRef
Known GenesSYT15
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2854902
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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