A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1665387



Internal ID12481819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45102290..45102290hg38UCSC Ensembl
chr11:45123841..45123841hg19UCSC Ensembl
chr11:45080417..45080417hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38132
hg19132
hg18132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4310258
SamplesHuRef
Known GenesPRDM11
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1665387
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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