A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664347



Internal ID9583766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57401519..57401924hg38UCSC Ensembl
chr14:57868237..57868642hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5811744
SamplesNA12749
Known GenesNAA30
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664347
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer