A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669637



Internal ID9589056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24274158..24318169hg38UCSC Ensembl
chr14:24743364..24787375hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3844012
hg1944012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6563684
SamplesHG00320
Known GenesCIDEB, DHRS1, LTB4R, LTB4R2, NOP9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669637
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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