A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668234



Internal ID9587653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12912028..12912442hg38UCSC Ensembl
chr19:13022842..13023256hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5868227, essv5806141, essv6486351, essv5545400, essv6408830, essv5666469, essv5953540, essv5618058
SamplesNA19704, NA18489, NA19663, NA18856, NA18909, NA19108, NA20348, NA19102
Known GenesSYCE2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668234
Frequency
Sample Size1151
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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