A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660568



Internal ID9579987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39876452..39906245hg38UCSC Ensembl
chr19:40367092..40399033hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3829794
hg1931942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6557249, essv5663522, essv5831049, essv6280087
SamplesNA19463, NA18934, NA20540, NA19750
Known GenesFCGBP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660568
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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