A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1662663



Internal ID12825781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103132008..103132068hg38UCSC Ensembl
chr14:103598345..103598405hg19UCSC Ensembl
chr14:102668098..102668158hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3861
hg1961
hg1861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4178082
SamplesHuRef
Known GenesTNFAIP2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1662663
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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