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nsv4512040

  • 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: 30 SVs from 8 studies. See in: genome view    
Remapped(Score: Perfect):37,921,838-37,921,838Question Mark
Overlapping variant regions from other studies: 30 SVs from 8 studies. See in: genome view    
Submitted genomic36,550,240-36,550,240Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4512040RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2037,921,83837,921,838
nsv4512040Submitted genomicGRCh37.p13Primary AssemblyNC_000020.10Chr2036,550,24036,550,240

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16033675alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16033675RemappedPerfectNC_000020.11:g.379
21838_37921839ins6
0
GRCh38.p12First PassNC_000020.11Chr2037,921,83837,921,838
nssv16033675Submitted genomicNC_000020.10:g.365
50240_36550241ins6
0
GRCh37.p13NC_000020.10Chr2036,550,24036,550,240

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)
nssv160336754.7e-005121340
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