A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1002859



Internal ID6714993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:12141064..12142862hg38UCSC Ensembl
Outerchr19:12251879..12253677hg19UCSC Ensembl
Outerchr19:12112879..12114677hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382721
hg192721
hg182721
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563569
SamplesHuRef
Known GenesZNF625-ZNF20
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1002859
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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