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nsv4321173

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:43,934,494

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 32240 SVs from 23 studies. See in: genome view    
Remapped(Score: Good):87,069,223-131,003,716Question Mark
Overlapping variant regions from other studies: 32204 SVs from 23 studies. See in: genome view    
Submitted genomic86,365,040-130,339,409Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4321173RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr587,069,223131,003,716
nsv4321173Submitted genomicGRCh37.p13Primary AssemblyNC_000005.9Chr586,365,040130,339,409

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091359inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091359RemappedGoodNC_000005.10:g.870
69223_131003716inv
GRCh38.p12First PassNC_000005.10Chr587,069,223131,003,716
nssv16091359Submitted genomicNC_000005.9:g.8636
5040_130339409inv
GRCh37.p13NC_000005.9Chr586,365,040130,339,409

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)
nssv160913594.6e-005121694
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