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nsv4569850

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:252,568

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 239 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):75,576,941-75,829,508Question Mark
Overlapping variant regions from other studies: 239 SVs from 16 studies. See in: genome view    
Submitted genomic73,573,022-73,825,589Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4569850RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1775,576,94175,829,508
nsv4569850Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1773,573,02273,825,589

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091093inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091093RemappedPerfectNC_000017.11:g.755
76941_75829508inv
GRCh38.p12First PassNC_000017.11Chr1775,576,94175,829,508
nssv16091093Submitted genomicNC_000017.10:g.735
73022_73825589inv
GRCh37.p13NC_000017.10Chr1773,573,02273,825,589

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)
nssv160910934.6e-005121694
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