A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1638e59



Internal ID22762858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75204569..75224377hg38UCSC Ensembl
chr16:75238467..75258275hg19UCSC Ensembl
chr16:73795968..73815776hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3819809
hg1919809
hg1819809
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3383927, esv3385328
SamplesNA12878
Known GenesCTRB1, CTRB2
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1638e59
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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