A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1092719



Internal ID12255843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65736013..65736013hg38UCSC Ensembl
chr11:65503484..65503484hg19UCSC Ensembl
chr11:65260060..65260060hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38314
hg19314
hg18314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3697472
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1092719
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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