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nsv5870436

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,104

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 214 SVs from 39 studies. See in: genome view    
Submitted genomic231,184,145-231,186,248Question Mark
Overlapping variant regions from other studies: 219 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):231,319,891-231,321,994Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5870436Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1231,184,145231,186,248
nsv5870436RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1231,319,891231,321,994

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17357420deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17357420Submitted genomicNC_000001.11:g.231
184145_231186248de
l
GRCh38 (hg38)NC_000001.11Chr1231,184,145231,186,248
nssv17357420RemappedPerfectNC_000001.10:g.231
319891_231321994de
l
GRCh37.p13First PassNC_000001.10Chr1231,319,891231,321,994

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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