A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv70e199



Internal ID22757843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152522701..152525439hg38UCSC Ensembl
chr1:152495177..152497915hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg382739
hg192739
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2657922, esv2671361
SamplesNA19921
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv70e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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