A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2838791



Internal ID10858488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:226300710..226306455hg38UCSC Ensembl
Outerchr2:227165426..227171171hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg385746
hg195746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7108358
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2838791
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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