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nsv5554565

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 72 SVs from 18 studies. See in: genome view    
Submitted genomic89,833,181-89,833,181Question Mark
Overlapping variant regions from other studies: 72 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):90,299,525-90,299,525Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5554565Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1489,833,18189,833,181
nsv5554565RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1490,299,52590,299,525

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17697156mobile element insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17697156Submitted genomicNC_000014.9:g.8983
3181_89833182ins26
2
GRCh38 (hg38)NC_000014.9Chr1489,833,18189,833,181
nssv17697156RemappedPerfectNC_000014.8:g.9029
9525_90299526ins26
2
GRCh37.p13First PassNC_000014.8Chr1490,299,52590,299,525

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)
nssv176971560.002156404
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