A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv622e199



Internal ID22758395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9163569..9175716hg38UCSC Ensembl
chr19:9274245..9286392hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3812148
hg1912148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2670216, esv2659174, esv2666361
SamplesHG00536, HG00187, NA20507, HG01522, NA20814, NA20796, NA18595, HG00346, HG00185, NA19904, HG00243, HG00512, HG00139, HG01072, NA18557, NA18908, NA12748, HG00188, NA18544, HG01515, NA18637, NA18534, NA19064, NA19000, NA06989, HG01148, NA20773, NA18941, NA18610, NA18549
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv622e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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