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nsv5539889

  • 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: 138 SVs from 25 studies. See in: genome view    
Submitted genomic70,403,589-70,403,589Question Mark
Overlapping variant regions from other studies: 138 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):70,797,369-70,797,369Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5539889Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1270,403,58970,403,589
nsv5539889RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1270,797,36970,797,369

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17688931insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17688931Submitted genomicNC_000012.12:g.704
03589_70403590ins1
94
GRCh38 (hg38)NC_000012.12Chr1270,403,58970,403,589
nssv17688931RemappedPerfectNC_000012.11:g.707
97369_70797370ins1
94
GRCh37.p13First PassNC_000012.11Chr1270,797,36970,797,369

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)
nssv17688931<0.00146382
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