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nsv5521630

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:109

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 113 SVs from 22 studies. See in: genome view    
Submitted genomic46,288,250-46,288,358Question Mark
Overlapping variant regions from other studies: 113 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):44,916,889-44,916,997Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5521630Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2046,288,25046,288,358
nsv5521630RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2044,916,88944,916,997

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17732665duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17732665Submitted genomicNC_000020.11:g.462
88250_46288358dup
GRCh38 (hg38)NC_000020.11Chr2046,288,25046,288,358
nssv17732665RemappedPerfectNC_000020.10:g.449
16889_44916997dup
GRCh37.p13First PassNC_000020.10Chr2044,916,88944,916,997

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)
nssv17732665<0.00116404
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