A curated catalogue of human genomic structural variation




Variant Details

Variant: esv988052



Internal ID7060352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98443876..98443876hg38UCSC Ensembl
chr13:99096130..99096130hg19UCSC Ensembl
chr13:97894131..97894131hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3858
hg1958
hg1858
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3577111
SamplesHuRef
Known GenesFARP1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv988052
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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