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nsv5420099

  • 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 16 studies. See in: genome view    
Submitted genomic31,221,399-31,221,450Question Mark
Overlapping variant regions from other studies: 86 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):31,617,385-31,617,436Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5420099Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2231,221,39931,221,450
nsv5420099RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2231,617,38531,617,436

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17728473alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17728473Submitted genomicNC_000022.11:g.312
21399_31221450ins2
79
GRCh38 (hg38)NC_000022.11Chr2231,221,39931,221,450
nssv17728473RemappedPerfectNC_000022.10:g.316
17385_31617436ins2
79
GRCh37.p13First PassNC_000022.10Chr2231,617,38531,617,436

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)
nssv17728473<0.00116404
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