A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661183



Internal ID9927288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15623236..15671327hg38UCSC Ensembl
Outerchr19:15623079..15671480hg38UCSC Ensembl
Innerchr19:15734046..15782137hg19UCSC Ensembl
Outerchr19:15733889..15782290hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3848402
hg1948402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv627e199
Supporting Variantsessv5637635, essv5847366, essv6278617
SamplesHG00337, HG01171, HG00479
Known GenesCYP4F3, CYP4F8
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661183
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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