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nsv4515437

  • 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: 26 SVs from 3 studies. See in: genome view    
Remapped(Score: Perfect):75,660,352-75,660,352Question Mark
Overlapping variant regions from other studies: 26 SVs from 3 studies. See in: genome view    
Submitted genomic76,126,695-76,126,695Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4515437RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1475,660,35275,660,352
nsv4515437Submitted genomicGRCh37.p13Primary AssemblyNC_000014.8Chr1476,126,69576,126,695

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16011039alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16011039RemappedPerfectNC_000014.9:g.7566
0352_75660353ins28
1
GRCh38.p12First PassNC_000014.9Chr1475,660,35275,660,352
nssv16011039Submitted genomicNC_000014.8:g.7612
6695_76126696ins28
1
GRCh37.p13NC_000014.8Chr1476,126,69576,126,695

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)
nssv160110394.6e-005121694
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