A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422467



Internal ID8253250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:62105992..62267614hg38UCSC Ensembl
Innerchr14:62572710..62734332hg19UCSC Ensembl
Innerchr14:61642463..61804085hg18UCSC Ensembl
Innerchr14:61642463..61804085hg17UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38161623
hg19161623
hg18161623
hg17161623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5161436
SamplesND03096
Known GenesLINC00643, LINC00644
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)esv2422467
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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