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nsv5418362

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 123 SVs from 23 studies. See in: genome view    
Submitted genomic46,393,998-46,394,062Question Mark
Overlapping variant regions from other studies: 123 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):46,859,670-46,859,734Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5418362Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr146,393,99846,394,062
nsv5418362RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr146,859,67046,859,734

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16901870duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16901870Submitted genomicNC_000001.11:g.463
93998_46394062dup
GRCh38 (hg38)NC_000001.11Chr146,393,99846,394,062
nssv16901870RemappedPerfectNC_000001.10:g.468
59670_46859734dup
GRCh37.p13First PassNC_000001.10Chr146,859,67046,859,734

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)
nssv169018700.013846398
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