A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5833894



Internal ID8811297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6907737..6908439hg38UCSC Ensembl
chr16:6957738..6958440hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38703
hg19703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657642
Supporting Variants
SamplesHG01079
Known GenesRBFOX1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5833894
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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