A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4178082



Internal ID11460620
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1662663
Supporting Variants
SamplesHuRef
Known GenesTNFAIP2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4178082
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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