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nsv6020279

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:77

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 90 SVs from 15 studies. See in: genome view    
Submitted genomic149,274,610-149,274,686Question Mark
Overlapping variant regions from other studies: 90 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):148,654,173-148,654,249Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6020279Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5149,274,610149,274,686
nsv6020279RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5148,654,173148,654,249

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17557882deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17557882Submitted genomicNC_000005.10:g.149
274610_149274686de
l
GRCh38 (hg38)NC_000005.10Chr5149,274,610149,274,686
nssv17557882RemappedPerfectNC_000005.9:g.1486
54173_148654249del
GRCh37.p13First PassNC_000005.9Chr5148,654,173148,654,249

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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