A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv120e199



Internal ID20123422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12077979..12082131hg38UCSC Ensembl
chr10:12119978..12124130hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg384153
hg194153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2658955, esv2663405
SamplesHG00285
Known GenesDHTKD1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv120e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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