A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564833



Internal ID7035933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105477270..105479324hg38UCSC Ensembl
Outerchr14:105943607..105945661hg19UCSC Ensembl
Outerchr14:105014652..105016706hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg382913
hg192913
hg182913
Variant TypeCNV insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1004211
Supporting Variants
SamplesHuRef
Known GenesCRIP2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564833
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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