A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632127



Internal ID7018937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:53902450..54111715hg38UCSC Ensembl
Innerchr13:53902640..54111525hg38UCSC Ensembl
Outerchr13:53902260..54111905hg38UCSC Ensembl
chr13:54476585..54685850hg19UCSC Ensembl
Innerchr13:54476775..54685660hg19UCSC Ensembl
Outerchr13:54476395..54686040hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38209266
hg19209266
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14733021, essv14733020, essv14733022, essv14733018, essv14733019
SamplesHG03009, HG04106, HG03990, HG04162, NA21113
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632127
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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