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nsv5474574

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,000

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 155 SVs from 22 studies. See in: genome view    
Submitted genomic81,667,805-81,669,804Question Mark
Overlapping variant regions from other studies: 155 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):82,580,040-82,582,039Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5474574Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr881,667,80581,669,804
nsv5474574RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr882,580,04082,582,039

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17013924deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17013924Submitted genomicNC_000008.11:g.816
67805_81669804del
GRCh38 (hg38)NC_000008.11Chr881,667,80581,669,804
nssv17013924RemappedPerfectNC_000008.10:g.825
80040_82582039del
GRCh37.p13First PassNC_000008.10Chr882,580,04082,582,039

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)
nssv17013924<0.00116404
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