A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600267



Internal ID6640531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38809373..38862827hg38UCSC Ensembl
Innerchr4:38809523..38862677hg38UCSC Ensembl
Outerchr4:38809223..38862977hg38UCSC Ensembl
chr4:38810994..38864448hg19UCSC Ensembl
Innerchr4:38811144..38864298hg19UCSC Ensembl
Outerchr4:38810844..38864598hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3853455
hg1953455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11397833
SamplesNA19473
Known GenesTLR6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600267
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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