A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643775



Internal ID7030533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15646813..15666335hg38UCSC Ensembl
Innerchr19:15646820..15666328hg38UCSC Ensembl
Outerchr19:15646806..15666342hg38UCSC Ensembl
chr19:15757623..15777145hg19UCSC Ensembl
Innerchr19:15757630..15777138hg19UCSC Ensembl
Outerchr19:15757616..15777152hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3819523
hg1919523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16000635
SamplesHG01813
Known GenesCYP4F3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643775
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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