A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3383927



Internal ID15230897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75204569..75222638hg38UCSC Ensembl
Innerchr16:75206559..75221058hg38UCSC Ensembl
Outerchr16:75204459..75222758hg38UCSC Ensembl
chr16:75238467..75256536hg19UCSC Ensembl
Innerchr16:75240457..75254956hg19UCSC Ensembl
Outerchr16:75238357..75256656hg19UCSC Ensembl
chr16:73795968..73814037hg18UCSC Ensembl
Innerchr16:73797958..73812457hg18UCSC Ensembl
Outerchr16:73795858..73814157hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3818070
hg1918070
hg1818070
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1638e59
Supporting Variantsessv8808766
SamplesNA12878
Known GenesCTRB1, CTRB2
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3383927
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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