A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6173949



Internal ID9781357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15615987..15674596hg38UCSC Ensembl
Outerchr19:15615953..15674631hg38UCSC Ensembl
Innerchr19:15726798..15785406hg19UCSC Ensembl
Outerchr19:15726764..15785441hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3858679
hg1958678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673235
Supporting Variants
SamplesNA19764
Known GenesCYP4F12, CYP4F3, CYP4F8
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6173949
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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