A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1580794



Internal ID12743915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62386485..62386485hg38UCSC Ensembl
chr11:62153957..62153957hg19UCSC Ensembl
chr11:61910533..61910533hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38121
hg19121
hg18121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3802509
SamplesHuRef
Known GenesASRGL1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1580794
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer