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nsv5537568

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:42

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 94 SVs from 20 studies. See in: genome view    
Submitted genomic85,631,122-85,631,163Question Mark
Overlapping variant regions from other studies: 94 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):86,097,466-86,097,507Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5537568Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1485,631,12285,631,163
nsv5537568RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1486,097,46686,097,507

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17697581insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17697581Submitted genomicNC_000014.9:g.8563
1122_85631163ins62
GRCh38 (hg38)NC_000014.9Chr1485,631,12285,631,163
nssv17697581RemappedPerfectNC_000014.8:g.8609
7466_86097507ins62
GRCh37.p13First PassNC_000014.8Chr1486,097,46686,097,507

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)
nssv17697581<0.00136404
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