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nsv3558511

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Description:Insertion of a L1 mobile element relative to the reference
  • Publication(s):Chaisson et al. 2019

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 391 SVs from 30 studies. See in: genome view    
Submitted genomic1,456,596-1,456,596Question Mark
Overlapping variant regions from other studies: 391 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):1,456,711-1,456,711Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv3558511Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr51,456,5961,456,596
nsv3558511RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr51,456,7111,456,711

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv14425578line1 insertionHG00514Optical mapping, SequencingOptical mapping, Sequence alignment, de novo and local sequence assembly39,861
nssv14467515line1 insertionSAMN00006581Optical mapping, SequencingOptical mapping, Sequence alignment, de novo and local sequence assembly41,185

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv14425578Submitted genomicNC_000005.10:g.145
6596_1456597ins60
GRCh38 (hg38)NC_000005.10Chr51,456,5961,456,596
nssv14467515Submitted genomicNC_000005.10:g.145
6596_1456597ins60
GRCh38 (hg38)NC_000005.10Chr51,456,5961,456,596
nssv14425578RemappedPerfectNC_000005.9:g.1456
711_1456712ins60
GRCh37.p13First PassNC_000005.9Chr51,456,7111,456,711
nssv14467515RemappedPerfectNC_000005.9:g.1456
711_1456712ins60
GRCh37.p13First PassNC_000005.9Chr51,456,7111,456,711

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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