A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1060e199



Internal ID20124362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178226303..178233781hg38UCSC Ensembl
chr5:177653304..177660782hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg387479
hg197479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2661450, esv2668543
SamplesHG00274
Known GenesPHYKPL
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1060e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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