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nsv5398498

  • 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: 77 SVs from 19 studies. See in: genome view    
Submitted genomic42,395,620-42,395,671Question Mark
Overlapping variant regions from other studies: 77 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):42,437,112-42,437,163Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5398498Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr342,395,62042,395,671
nsv5398498RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr342,437,11242,437,163

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16933643alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16933643Submitted genomicNC_000003.12:g.423
95620_42395671ins2
80
GRCh38 (hg38)NC_000003.12Chr342,395,62042,395,671
nssv16933643RemappedPerfectNC_000003.11:g.424
37112_42437163ins2
80
GRCh37.p13First PassNC_000003.11Chr342,437,11242,437,163

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)
nssv16933643<0.00116404
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