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nsv5543590

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:39

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 130 SVs from 25 studies. See in: genome view    
Submitted genomic52,031,339-52,031,377Question Mark
Overlapping variant regions from other studies: 130 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):52,497,011-52,497,049Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5543590Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr152,031,33952,031,377
nsv5543590RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr152,497,01152,497,049

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16902763insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16902763Submitted genomicNC_000001.11:g.520
31339_52031377ins1
89
GRCh38 (hg38)NC_000001.11Chr152,031,33952,031,377
nssv16902763RemappedPerfectNC_000001.10:g.524
97011_52497049ins1
89
GRCh37.p13First PassNC_000001.10Chr152,497,01152,497,049

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)
nssv16902763<0.00166404
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