A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2896012



Internal ID10568992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:46461865..46467865hg38UCSC Ensembl
Innerchr13:47036000..47042000hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7165579
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2896012
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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