A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv324e199



Internal ID18982378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122408946..122411321hg38UCSC Ensembl
chr12:122893493..122895868hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg382376
hg192376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2673330, esv2670426
SamplesHG01051
Known GenesCLIP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv324e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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