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nsv5950515

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:102

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 94 SVs from 15 studies. See in: genome view    
Submitted genomic20,442,912-20,443,013Question Mark
Overlapping variant regions from other studies: 94 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):20,423,556-20,423,657Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5950515Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2020,442,91220,443,013
nsv5950515RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2020,423,55620,423,657

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17393233deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17393233Submitted genomicNC_000020.11:g.204
42912_20443013del
GRCh38 (hg38)NC_000020.11Chr2020,442,91220,443,013
nssv17393233RemappedPerfectNC_000020.10:g.204
23556_20423657del
GRCh37.p13First PassNC_000020.10Chr2020,423,55620,423,657

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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