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nsv5416566

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 126 SVs from 22 studies. See in: genome view    
Submitted genomic1,145,480-1,145,531Question Mark
Overlapping variant regions from other studies: 126 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):1,126,123-1,126,174Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5416566Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr201,145,4801,145,531
nsv5416566RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr201,126,1231,126,174

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17730237alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17730237Submitted genomicNC_000020.11:g.114
5480_1145531ins280
GRCh38 (hg38)NC_000020.11Chr201,145,4801,145,531
nssv17730237RemappedPerfectNC_000020.10:g.112
6123_1126174ins280
GRCh37.p13First PassNC_000020.10Chr201,126,1231,126,174

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17730237<0.00116404
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