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nsv4564128

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:74,342,946

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 51745 SVs from 26 studies. See in: genome view    
Remapped(Score: Good):3,432,363-77,775,308Question Mark
Overlapping variant regions from other studies: 51682 SVs from 26 studies. See in: genome view    
Submitted genomic3,474,047-77,824,459Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4564128RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr33,432,36377,775,308
nsv4564128Submitted genomicGRCh37.p13Primary AssemblyNC_000003.11Chr33,474,04777,824,459

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091156inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091156RemappedGoodNC_000003.12:g.343
2363_77775308inv
GRCh38.p12First PassNC_000003.12Chr33,432,36377,775,308
nssv16091156Submitted genomicNC_000003.11:g.347
4047_77824459inv
GRCh37.p13NC_000003.11Chr33,474,04777,824,459

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)
nssv160911564.6e-005121694
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