A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5504733



Internal ID8482136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89362422..89362478hg38UCSC Ensembl
Outerchr14:89362051..89362848hg38UCSC Ensembl
Innerchr14:89828766..89828822hg19UCSC Ensembl
Outerchr14:89828395..89829192hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2668092
Supporting Variants
SamplesNA19462
Known GenesFOXN3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5504733
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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