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nsv4328719

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35,685

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 45 SVs from 12 studies. See in: genome view    
Remapped(Score: Perfect):27,988,330-28,024,014Question Mark
Overlapping variant regions from other studies: 45 SVs from 12 studies. See in: genome view    
Submitted genomic26,315,356-26,351,040Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4328719RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1727,988,33028,024,014
nsv4328719Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1726,315,35626,351,040

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091081inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091081RemappedPerfectNC_000017.11:g.279
88330_28024014inv
GRCh38.p12First PassNC_000017.11Chr1727,988,33028,024,014
nssv16091081Submitted genomicNC_000017.10:g.263
15356_26351040inv
GRCh37.p13NC_000017.10Chr1726,315,35626,351,040

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)
nssv160910814.6e-005121694
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