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nsv4322553

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,183,675

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 12613 SVs from 27 studies. See in: genome view    
Remapped(Score: Good):16,541,107-31,724,781Question Mark
Overlapping variant regions from other studies: 12608 SVs from 27 studies. See in: genome view    
Submitted genomic16,634,964-31,736,102Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4322553RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1616,541,10731,724,781
nsv4322553Submitted genomicGRCh37.p13Primary AssemblyNC_000016.9Chr1616,634,96431,736,102

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091061inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091061RemappedGoodNC_000016.10:g.165
41107_31724781inv
GRCh38.p12First PassNC_000016.10Chr1616,541,10731,724,781
nssv16091061Submitted genomicNC_000016.9:g.1663
4964_31736102inv
GRCh37.p13NC_000016.9Chr1616,634,96431,736,102

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)
nssv160910614.6e-005121694
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