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nsv4460550

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 32 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):201,936,310-201,936,310Question Mark
Overlapping variant regions from other studies: 32 SVs from 6 studies. See in: genome view    
Submitted genomic201,905,438-201,905,438Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4460550RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1201,936,310201,936,310
nsv4460550Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr1201,905,438201,905,438

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16028788alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16028788RemappedPerfectNC_000001.11:g.201
936310_201936311in
s280
GRCh38.p12First PassNC_000001.11Chr1201,936,310201,936,310
nssv16028788Submitted genomicNC_000001.10:g.201
905438_201905439in
s280
GRCh37.p13NC_000001.10Chr1201,905,438201,905,438

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)
nssv160287889.2e-005221692
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