A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv20n50



Internal ID22767849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75204640..75224276hg38UCSC Ensembl
chr16:75238538..75258174hg19UCSC Ensembl
chr16:73796039..73815675hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3819637
hg1919637
hg1819637
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv513707, nsv513708
Samples1
Known GenesCTRB1, CTRB2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)dgv20n50
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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