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nsv5726374

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Description:Insertion of a SVA mobile element relative to the reference
  • Publication(s):Chuang et al. 2021

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 266 SVs from 38 studies. See in: genome view    
Submitted genomic74,580,918-74,580,918Question Mark
Overlapping variant regions from other studies: 266 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):72,577,057-72,577,057Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5726374Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1774,580,91874,580,918
nsv5726374RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1772,577,05772,577,057

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17246609sva insertionSequencingOther
nssv17251562sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17246609Submitted genomicNC_000017.11:g.745
80918_74580919ins4
79
GRCh38 (hg38)NC_000017.11Chr1774,580,91874,580,918
nssv17251562Submitted genomicNC_000017.11:g.745
80918_74580919ins4
79
GRCh38 (hg38)NC_000017.11Chr1774,580,91874,580,918
nssv17246609RemappedPerfectNC_000017.10:g.725
77057_72577058ins4
79
GRCh37.p13First PassNC_000017.10Chr1772,577,05772,577,057
nssv17251562RemappedPerfectNC_000017.10:g.725
77057_72577058ins4
79
GRCh37.p13First PassNC_000017.10Chr1772,577,05772,577,057

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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