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nsv4492585

  • 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: 56 SVs from 4 studies. See in: genome view    
Remapped(Score: Perfect):3,741,414-3,741,414Question Mark
Overlapping variant regions from other studies: 56 SVs from 4 studies. See in: genome view    
Submitted genomic3,741,648-3,741,648Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4492585RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr63,741,4143,741,414
nsv4492585Submitted genomicGRCh37.p13Primary AssemblyNC_000006.11Chr63,741,6483,741,648

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16066304alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16066304RemappedPerfectNC_000006.12:g.374
1414_3741415ins279
GRCh38.p12First PassNC_000006.12Chr63,741,4143,741,414
nssv16066304Submitted genomicNC_000006.11:g.374
1648_3741649ins279
GRCh37.p13NC_000006.11Chr63,741,6483,741,648

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)
nssv16066304<0.001421694
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