A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662224



Internal ID9928329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9938030..9938982hg38UCSC Ensembl
chr19:10048706..10049658hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38953
hg19953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5551430, essv5438643, essv5757946, essv6360265, essv6222621, essv5996041, essv6297730, essv5919740, essv5617411, essv5680740, essv5791210, essv5993000
SamplesNA19332, NA19446, NA19457, NA18868, NA19371, NA18516, NA19712, NA19467, NA19328, NA20334, NA18487, NA19431
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662224
Frequency
Sample Size1151
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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