A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1342891



Internal ID12506013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107391212..107391212hg38UCSC Ensembl
chr3:107110059..107110059hg19UCSC Ensembl
chr3:108592749..108592749hg18UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3899
hg1999
hg1899
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3752821
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1342891
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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