A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv627e199



Internal ID22758400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15615949..15676977hg38UCSC Ensembl
chr19:15726760..15787787hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3861029
hg1961028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2664037, esv2673235, esv2657942, esv2661183, esv2673421
SamplesHG00337, NA19764, NA20768, HG01171, HG00245, HG00479, NA07051
Known GenesCYP4F12, CYP4F3, CYP4F8
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv627e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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