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nsv4538626

  • 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: 19 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):56,897,114-56,897,114Question Mark
Overlapping variant regions from other studies: 18 SVs from 5 studies. See in: genome view    
Submitted genomic54,974,475-54,974,475Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4538626RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1756,897,11456,897,114
nsv4538626Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1754,974,47554,974,475

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16018648insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16018648RemappedPerfectNC_000017.11:g.568
97114_56897115ins3
37
GRCh38.p12First PassNC_000017.11Chr1756,897,11456,897,114
nssv16018648Submitted genomicNC_000017.10:g.549
74475_54974476ins3
37
GRCh37.p13NC_000017.10Chr1754,974,47554,974,475

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)
nssv160186480.0012421688
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