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nsv5718445

  • 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: 167 SVs from 26 studies. See in: genome view    
Submitted genomic60,414,608-60,414,608Question Mark
Overlapping variant regions from other studies: 167 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):58,491,969-58,491,969Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5718445Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1760,414,60860,414,608
nsv5718445RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1758,491,96958,491,969

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17237777sva insertionSequencingOther
nssv17245355sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17237777Submitted genomicNC_000017.11:g.604
14608_60414609ins1
240
GRCh38 (hg38)NC_000017.11Chr1760,414,60860,414,608
nssv17245355Submitted genomicNC_000017.11:g.604
14608_60414609ins1
240
GRCh38 (hg38)NC_000017.11Chr1760,414,60860,414,608
nssv17237777RemappedPerfectNC_000017.10:g.584
91969_58491970ins1
240
GRCh37.p13First PassNC_000017.10Chr1758,491,96958,491,969
nssv17245355RemappedPerfectNC_000017.10:g.584
91969_58491970ins1
240
GRCh37.p13First PassNC_000017.10Chr1758,491,96958,491,969

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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