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nsv5413995

  • 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: 86 SVs from 27 studies. See in: genome view    
Submitted genomic51,247,073-51,247,124Question Mark
Overlapping variant regions from other studies: 86 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):51,640,857-51,640,908Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5413995Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1251,247,07351,247,124
nsv5413995RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1251,640,85751,640,908

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058576alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058576Submitted genomicNC_000012.12:g.512
47073_51247124ins2
80
GRCh38 (hg38)NC_000012.12Chr1251,247,07351,247,124
nssv17058576RemappedPerfectNC_000012.11:g.516
40857_51640908ins2
80
GRCh37.p13First PassNC_000012.11Chr1251,640,85751,640,908

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)
nssv17058576<0.00116404
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