A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv86e199



Internal ID22757859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:196661896..196663989hg38UCSC Ensembl
chr1:196631026..196633119hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg382094
hg192094
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2660886, esv2677344
SamplesNA19704
Known GenesCFH
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv86e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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