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nsv5408197

  • 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: 75 SVs from 23 studies. See in: genome view    
Submitted genomic40,431,110-40,431,161Question Mark
Overlapping variant regions from other studies: 75 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):40,472,601-40,472,652Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5408197Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr340,431,11040,431,161
nsv5408197RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr340,472,60140,472,652

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16932300alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16932300Submitted genomicNC_000003.12:g.404
31110_40431161ins2
80
GRCh38 (hg38)NC_000003.12Chr340,431,11040,431,161
nssv16932300RemappedPerfectNC_000003.11:g.404
72601_40472652ins2
80
GRCh37.p13First PassNC_000003.11Chr340,472,60140,472,652

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)
nssv16932300<0.00126404
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