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nsv5406109

  • 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: 137 SVs from 21 studies. See in: genome view    
Submitted genomic37,359,200-37,359,251Question Mark
Overlapping variant regions from other studies: 137 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):37,586,343-37,586,394Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5406109Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr237,359,20037,359,251
nsv5406109RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr237,586,34337,586,394

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16911481alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16911481Submitted genomicNC_000002.12:g.373
59200_37359251ins2
80
GRCh38 (hg38)NC_000002.12Chr237,359,20037,359,251
nssv16911481RemappedPerfectNC_000002.11:g.375
86343_37586394ins2
80
GRCh37.p13First PassNC_000002.11Chr237,586,34337,586,394

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)
nssv169114810.003176404
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