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nsv4052544

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 36 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):201,412,421-201,412,485Question Mark
Overlapping variant regions from other studies: 36 SVs from 6 studies. See in: genome view    
Submitted genomic201,381,549-201,381,613Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4052544RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1201,412,421201,412,485
nsv4052544Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr1201,381,549201,381,613

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15964061duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15964061RemappedPerfectNC_000001.11:g.201
412421_201412485du
p
GRCh38.p12First PassNC_000001.11Chr1201,412,421201,412,485
nssv15964061Submitted genomicNC_000001.10:g.201
381549_201381613du
p
GRCh37.p13NC_000001.10Chr1201,381,549201,381,613

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv15964061<0.001321692
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