A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7111470



Internal ID10389752
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 StatusS
Merged Variantsesv2841903
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7111470
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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