A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1063774



Internal ID11880213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14841729..14841729hg38UCSC Ensembl
chr11:14863275..14863275hg19UCSC Ensembl
chr11:14819851..14819851hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381063
hg191063
hg181063
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4241462
SamplesHuRef
Known GenesPDE3B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1063774
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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