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nsv5447926

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:54

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 86 SVs from 20 studies. See in: genome view    
Submitted genomic45,121,260-45,121,313Question Mark
Overlapping variant regions from other studies: 86 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):45,162,752-45,162,805Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5447926Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr345,121,26045,121,313
nsv5447926RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr345,162,75245,162,805

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16933692deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16933692Submitted genomicNC_000003.12:g.451
21260_45121313del
GRCh38 (hg38)NC_000003.12Chr345,121,26045,121,313
nssv16933692RemappedPerfectNC_000003.11:g.451
62752_45162805del
GRCh37.p13First PassNC_000003.11Chr345,162,75245,162,805

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)
nssv16933692<0.00116404
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