A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2861568



Internal ID10881265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125899431..125927431hg38UCSC Ensembl
Innerchr10:127588000..127616000hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3828001
hg1928001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7131135
SamplesHuRef
Known GenesFANK1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2861568
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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