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nsv3565886

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Description:Insertion of a Alu 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: 278 SVs from 49 studies. See in: genome view    
Submitted genomic29,103,296-29,103,326Question Mark
Overlapping variant regions from other studies: 284 SVs from 50 studies. See in: genome view    
Remapped(Score: Perfect):29,103,294-29,103,324Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv3565886Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr929,103,311 (-15, +15)29,103,311 (-15, +15)
nsv3565886RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr929,103,309 (-15, +15)29,103,309 (-15, +15)

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisZygosityOther Calls in this Sample and Study
nssv14346699alu insertionSAMN00006580SequencingSequence alignmentHeterozygous14,212

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv14346699Submitted genomicNC_000009.12:g.(29
103296_29103326)_(
29103296_29103326)
ins281
GRCh38 (hg38)NC_000009.12Chr929,103,311 (-15, +15)29,103,311 (-15, +15)
nssv14346699RemappedPerfectNC_000009.11:g.(29
103294_29103324)_(
29103294_29103324)
ins281
GRCh37.p13First PassNC_000009.11Chr929,103,309 (-15, +15)29,103,309 (-15, +15)

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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