A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv40e199



Internal ID22757813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40602678..40619089hg38UCSC Ensembl
chr1:41068350..41084761hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3816412
hg1916412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2658015, esv2665462
SamplesHG00237
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv40e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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