A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv564e199



Internal ID22758337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72384137..72388501hg38UCSC Ensembl
chr17:70380278..70384642hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg384365
hg194365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2672850, esv2656523
SamplesHG00671
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv564e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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