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nsv4330632

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:55,110,938

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 40997 SVs from 28 studies. See in: genome view    
Remapped(Score: Good):18,935,213-74,046,150Question Mark
Overlapping variant regions from other studies: 38902 SVs from 28 studies. See in: genome view    
Submitted genomic18,838,526-72,042,289Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4330632RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1718,935,21374,046,150
nsv4330632Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1718,838,52672,042,289

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091079inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091079RemappedGoodNC_000017.11:g.189
35213_74046150inv
GRCh38.p12First PassNC_000017.11Chr1718,935,21374,046,150
nssv16091079Submitted genomicNC_000017.10:g.188
38526_72042289inv
GRCh37.p13NC_000017.10Chr1718,838,52672,042,289

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)
nssv160910794.6e-005121694
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