A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv745e199



Internal ID22758518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165813130..165817802hg38UCSC Ensembl
chr2:166669640..166674312hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg384673
hg194673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2673437, esv2669102
SamplesNA18622
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv745e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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