A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv585e199



Internal ID20123887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22619158..22888354hg38UCSC Ensembl
chr18:20199121..20468317hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38269197
hg19269197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2671542, esv2660054
SamplesHG01102, NA19713
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv585e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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