A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1763444



Internal ID12579876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14161139..14161139hg38UCSC Ensembl
chr11:14182685..14182685hg19UCSC Ensembl
chr11:14139261..14139261hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4081195
SamplesHuRef
Known GenesSPON1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1763444
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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