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nsv5523535

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:302

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 115 SVs from 21 studies. See in: genome view    
Submitted genomic50,229,239-50,229,540Question Mark
Overlapping variant regions from other studies: 115 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):50,521,436-50,521,737Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5523535Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1550,229,23950,229,540
nsv5523535RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1550,521,43650,521,737

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17703075duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17703075Submitted genomicNC_000015.10:g.502
29239_50229540dup
GRCh38 (hg38)NC_000015.10Chr1550,229,23950,229,540
nssv17703075RemappedPerfectNC_000015.9:g.5052
1436_50521737dup
GRCh37.p13First PassNC_000015.9Chr1550,521,43650,521,737

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)
nssv17703075<0.00126404
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