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nsv5458099

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,679

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 85 SVs from 22 studies. See in: genome view    
Submitted genomic55,531,545-55,533,223Question Mark
Overlapping variant regions from other studies: 85 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):56,397,712-56,399,390Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5458099Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr455,531,54555,533,223
nsv5458099RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr456,397,71256,399,390

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16948991deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16948991Submitted genomicNC_000004.12:g.555
31545_55533223del
GRCh38 (hg38)NC_000004.12Chr455,531,54555,533,223
nssv16948991RemappedPerfectNC_000004.11:g.563
97712_56399390del
GRCh37.p13First PassNC_000004.11Chr456,397,71256,399,390

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)
nssv16948991<0.00126404
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