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nsv5487891

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:99,446

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 513 SVs from 66 studies. See in: genome view    
Submitted genomic52,930,374-53,029,819Question Mark
Overlapping variant regions from other studies: 513 SVs from 66 studies. See in: genome view    
Remapped(Score: Perfect):53,842,934-53,942,379Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5487891Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr852,930,37453,029,819
nsv5487891RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr853,842,93453,942,379

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17011064duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17011064Submitted genomicNC_000008.11:g.529
30374_53029819dup
GRCh38 (hg38)NC_000008.11Chr852,930,37453,029,819
nssv17011064RemappedPerfectNC_000008.10:g.538
42934_53942379dup
GRCh37.p13First PassNC_000008.10Chr853,842,93453,942,379

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)
nssv17011064<0.00116404
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