A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7364468



Internal ID10296064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:14621533..14623330hg38UCSC Ensembl
Outerchr19:14732345..14734142hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381798
hg191798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3094901
Supporting Variants
SamplesHuRef
Known GenesEMR3
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7364468
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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