A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6000606



Internal ID9213000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15616197..15674533hg38UCSC Ensembl
chr19:15727008..15785343hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3858337
hg1958336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664037
Supporting Variants
SamplesNA07051
Known GenesCYP4F12, CYP4F3, CYP4F8
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6000606
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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