A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513708



Internal ID15853129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75206191..75224276hg38UCSC Ensembl
Outerchr16:75240089..75258174hg19UCSC Ensembl
Outerchr16:73797590..73815675hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3818086
hg1918086
hg1818086
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv20n50
Supporting Variantsnssv626960
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)nsv513708
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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