A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7124581



Internal ID10056177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:1142021..1142275hg38UCSC Ensembl
Outerchr19:1142020..1142274hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2855014
Supporting Variants
SamplesHuRef
Known GenesSBNO2
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7124581
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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