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nsv3565896

  • 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: 190 SVs from 26 studies. See in: genome view    
Submitted genomic38,325,945-38,325,975Question Mark
Overlapping variant regions from other studies: 197 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):38,325,942-38,325,972Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv3565896Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr938,325,960 (-15, +15)38,325,960 (-15, +15)
nsv3565896RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr938,325,957 (-15, +15)38,325,957 (-15, +15)

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisZygosityOther Calls in this Sample and Study
nssv14346537alu insertionSAMN00006580SequencingSequence alignmentHeterozygous14,212

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv14346537Submitted genomicNC_000009.12:g.(38
325945_38325975)_(
38325945_38325975)
ins279
GRCh38 (hg38)NC_000009.12Chr938,325,960 (-15, +15)38,325,960 (-15, +15)
nssv14346537RemappedPerfectNC_000009.11:g.(38
325942_38325972)_(
38325942_38325972)
ins279
GRCh37.p13First PassNC_000009.11Chr938,325,957 (-15, +15)38,325,957 (-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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