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nsv5326663

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,099

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 284 SVs from 60 studies. See in: genome view    
Submitted genomic128,452,922-128,459,020Question Mark
Overlapping variant regions from other studies: 284 SVs from 60 studies. See in: genome view    
Remapped(Score: Perfect):129,465,168-129,471,266Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5326663Submitted genomicGRCh38.p13Primary AssemblyNC_000008.11Chr8128,452,922128,459,020
nsv5326663RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8129,465,168129,471,266

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16756240line1 deletionSequencingSplit read and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16756240Submitted genomicNC_000008.11:g.128
452922_128459020de
l
GRCh38.p13NC_000008.11Chr8128,452,922128,459,020
nssv16756240RemappedPerfectNC_000008.10:g.129
465168_129471266de
l
GRCh37.p13First PassNC_000008.10Chr8129,465,168129,471,266

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)
nssv167562400.993
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