A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2854680



Internal ID10874377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:43679208..43679796hg38UCSC Ensembl
Outerchr19:44183360..44183948hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38589
hg19589
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7124247
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2854680
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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