A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv129e199



Internal ID22757902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35405998..35410283hg38UCSC Ensembl
chr10:35694926..35699211hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg384286
hg194286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2674753, esv2677075
SamplesNA19713
Known GenesCCNY
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv129e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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