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nsv5534594

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:243

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 182 SVs from 26 studies. See in: genome view    
Submitted genomic53,206,256-53,206,498Question Mark
Overlapping variant regions from other studies: 182 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):50,732,626-50,732,868Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5534594Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1853,206,25653,206,498
nsv5534594RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1850,732,62650,732,868

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17718251insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17718251Submitted genomicNC_000018.10:g.532
06256_53206498ins1
91
GRCh38 (hg38)NC_000018.10Chr1853,206,25653,206,498
nssv17718251RemappedPerfectNC_000018.9:g.5073
2626_50732868ins19
1
GRCh37.p13First PassNC_000018.9Chr1850,732,62650,732,868

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)
nssv177182510.17710065698
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