nsv4514654

  • 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: 39 SVs from 4 studies. See in: genome view    
Remapped(Score: Perfect):55,565,836-55,565,836Question Mark
Overlapping variant regions from other studies: 39 SVs from 4 studies. See in: genome view    
Submitted genomic55,599,748-55,599,748Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4514654RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1655,565,83655,565,836
nsv4514654Submitted genomicGRCh37.p13Primary AssemblyNC_000016.9Chr1655,599,74855,599,748

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16014072alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16014072RemappedPerfectNC_000016.10:g.555
65836_55565837ins2
79
GRCh38.p12First PassNC_000016.10Chr1655,565,83655,565,836
nssv16014072Submitted genomicNC_000016.9:g.5559
9748_55599749ins27
9
GRCh37.p13NC_000016.9Chr1655,599,74855,599,748

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)
nssv160140724.6e-005121694
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