A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2841903



Internal ID10861600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:134209132..134212562hg38UCSC Ensembl
Outerchr2:134966703..134970133hg19UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg383431
hg193431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7111470
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2841903
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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