A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1148e199



Internal ID22758921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:103173639..103201313hg38UCSC Ensembl
chr6:103621514..103649188hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3827675
hg1927675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2672112, esv2671762
SamplesHG00139
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1148e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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