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nsv5430756

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:64

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 150 SVs from 23 studies. See in: genome view    
Submitted genomic80,871,760-80,871,823Question Mark
Overlapping variant regions from other studies: 150 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):78,845,560-78,845,623Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5430756Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1780,871,76080,871,823
nsv5430756RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1778,845,56078,845,623

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17715039alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17715039Submitted genomicNC_000017.11:g.808
71760_80871823ins2
79
GRCh38 (hg38)NC_000017.11Chr1780,871,76080,871,823
nssv17715039RemappedPerfectNC_000017.10:g.788
45560_78845623ins2
79
GRCh37.p13First PassNC_000017.10Chr1778,845,56078,845,623

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)
nssv177150390.002116404
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