A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5859662



Internal ID9742493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28648423..28649346hg38UCSC Ensembl
chr14:29117629..29118552hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38924
hg19924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673510
Supporting Variants
SamplesNA19678
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5859662
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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