A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668675



Internal ID9934780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:84866441..85249749hg38UCSC Ensembl
chr14:85332785..85716093hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38383309
hg19383309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6240397, essv6054732, essv5472176, essv5413340, essv5466381, essv5920085, essv6459853, essv6360664, essv6093476, essv6374368, essv6388648, essv5862346
SamplesNA20761, NA19350, NA20805, NA18870, NA19087, NA18908, NA19059, NA18950, NA19835, NA20803, NA18610, NA19472
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668675
Frequency
Sample Size1151
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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