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nsv5433286

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:58

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 170 SVs from 36 studies. See in: genome view    
Submitted genomic62,240,037-62,240,094Question Mark
Overlapping variant regions from other studies: 170 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):60,317,398-60,317,455Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5433286Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1762,240,03762,240,094
nsv5433286RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1760,317,39860,317,455

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17725000alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17725000Submitted genomicNC_000017.11:g.622
40037_62240094ins2
79
GRCh38 (hg38)NC_000017.11Chr1762,240,03762,240,094
nssv17725000RemappedPerfectNC_000017.10:g.603
17398_60317455ins2
79
GRCh37.p13First PassNC_000017.10Chr1760,317,39860,317,455

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)
nssv177250000.003216382
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