A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660886



Internal ID9926991
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 Variantsdgv86e199
Supporting Variantsessv5496125
SamplesNA19704
Known GenesCFH
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660886
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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