A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv151e199



Internal ID22757924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68852253..68864038hg38UCSC Ensembl
chr10:70612009..70623794hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3811786
hg1911786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2668546, esv2660031
SamplesHG01066, NA19315
Known GenesSTOX1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv151e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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