A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv625e199



Internal ID20123927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14538944..14542502hg38UCSC Ensembl
chr19:14649756..14653314hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg383559
hg193559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2678628, esv2675493
SamplesNA18868
Known GenesTECR
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv625e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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