A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663038



Internal ID9582457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3528688..3528856hg38UCSC Ensembl
chr19:3528686..3528854hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5488347, essv5408332, essv6431608, essv6053978, essv5761937, essv6129167, essv6483685, essv5789999, essv6270914, essv5685261, essv5424990, essv5761546, essv5467882, essv5534049, essv6053250, essv6092979
SamplesHG01441, NA11931, NA19359, HG01188, NA20322, NA20356, HG00140, NA19197, HG01047, NA19380, NA06986, NA20756, NA20332, NA19394, HG00345, HG00278
Known GenesFZR1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663038
Frequency
Sample Size1151
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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