A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1680226



Internal ID12843344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39469349..39469349hg38UCSC Ensembl
chr3:39510840..39510840hg19UCSC Ensembl
chr3:39485844..39485844hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3852
hg1952
hg1852
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3999555
SamplesHuRef
Known GenesMOBP
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1680226
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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