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nsv5501460

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:115

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 181 SVs from 24 studies. See in: genome view    
Submitted genomic49,767,994-49,768,108Question Mark
Overlapping variant regions from other studies: 181 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):50,342,130-50,342,244Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5501460Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1349,767,99449,768,108
nsv5501460RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1350,342,13050,342,244

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17687658duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17687658Submitted genomicNC_000013.11:g.497
67994_49768108dup
GRCh38 (hg38)NC_000013.11Chr1349,767,99449,768,108
nssv17687658RemappedPerfectNC_000013.10:g.503
42130_50342244dup
GRCh37.p13First PassNC_000013.10Chr1350,342,13050,342,244

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)
nssv17687658<0.00116404
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