A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1002029



Internal ID6714164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:1156440..1162872hg38UCSC Ensembl
Outerchr19:1156439..1162871hg19UCSC Ensembl
Outerchr19:1107439..1113871hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3810209
hg1910209
hg1810209
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563796
SamplesHuRef
Known GenesSBNO2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1002029
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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