A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659719



Internal ID9925824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75317928..75319282hg38UCSC Ensembl
chr14:75784631..75785985hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381355
hg191355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv403e199
Supporting Variantsessv5921417, essv6358307
SamplesNA19435, NA18873
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659719
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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