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nsv4557390

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 20 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):41,334,563-41,334,563Question Mark
Overlapping variant regions from other studies: 20 SVs from 5 studies. See in: genome view    
Submitted genomic41,302,301-41,302,301Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4557390RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr641,334,56341,334,563
nsv4557390Submitted genomicGRCh37.p13Primary AssemblyNC_000006.11Chr641,302,30141,302,301

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16066705line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16066705RemappedPerfectNC_000006.12:g.413
34563_41334564ins6
019
GRCh38.p12First PassNC_000006.12Chr641,334,56341,334,563
nssv16066705Submitted genomicNC_000006.11:g.413
02301_41302302ins6
019
GRCh37.p13NC_000006.11Chr641,302,30141,302,301

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)
nssv160667054.6e-005121694
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