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nsv5559816

  • 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: 170 SVs from 22 studies. See in: genome view    
Submitted genomic50,945,398-50,945,449Question Mark
Overlapping variant regions from other studies: 170 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):51,519,534-51,519,585Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5559816Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1350,945,39850,945,449
nsv5559816RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1351,519,53451,519,585

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17687726line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17687726Submitted genomicNC_000013.11:g.509
45398_50945449ins6
019
GRCh38 (hg38)NC_000013.11Chr1350,945,39850,945,449
nssv17687726RemappedPerfectNC_000013.10:g.515
19534_51519585ins6
019
GRCh37.p13First PassNC_000013.10Chr1351,519,53451,519,585

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)
nssv17687726<0.00116404
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