A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3387235



Internal ID15234204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26336547..26339599hg38UCSC Ensembl
Innerchr16:26338019..26338537hg38UCSC Ensembl
Outerchr16:26336437..26339719hg38UCSC Ensembl
chr16:26347868..26350920hg19UCSC Ensembl
Innerchr16:26349340..26349858hg19UCSC Ensembl
Outerchr16:26347758..26351040hg19UCSC Ensembl
chr16:26255369..26258421hg18UCSC Ensembl
Innerchr16:26257359..26256841hg18UCSC Ensembl
Outerchr16:26255259..26258541hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg383053
hg193053
hg183053
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8808722
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3387235
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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