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nsv5705669

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Description:Insertion of a Alu 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: 94 SVs from 22 studies. See in: genome view    
Submitted genomic81,491,944-81,491,944Question Mark
Overlapping variant regions from other studies: 94 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):81,958,288-81,958,288Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5705669Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1481,491,94481,491,944
nsv5705669RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1481,958,28881,958,288

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17196624alu insertionSequencingOther
nssv17227141alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17196624Submitted genomicNC_000014.9:g.8149
1944_81491945ins28
1
GRCh38 (hg38)NC_000014.9Chr1481,491,94481,491,944
nssv17227141Submitted genomicNC_000014.9:g.8149
1944_81491945ins28
1
GRCh38 (hg38)NC_000014.9Chr1481,491,94481,491,944
nssv17196624RemappedPerfectNC_000014.8:g.8195
8288_81958289ins28
1
GRCh37.p13First PassNC_000014.8Chr1481,958,28881,958,288
nssv17227141RemappedPerfectNC_000014.8:g.8195
8288_81958289ins28
1
GRCh37.p13First PassNC_000014.8Chr1481,958,28881,958,288

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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