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nsv4327395

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:67,998,117

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 46176 SVs from 25 studies. See in: genome view    
Remapped(Score: Good):126,546,726-194,544,842Question Mark
Overlapping variant regions from other studies: 46155 SVs from 25 studies. See in: genome view    
Submitted genomic126,265,569-194,265,571Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4327395RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3126,546,726194,544,842
nsv4327395Submitted genomicGRCh37.p13Primary AssemblyNC_000003.11Chr3126,265,569194,265,571

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091191inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091191RemappedGoodNC_000003.12:g.126
546726_194544842in
v
GRCh38.p12First PassNC_000003.12Chr3126,546,726194,544,842
nssv16091191Submitted genomicNC_000003.11:g.126
265569_194265571in
v
GRCh37.p13NC_000003.11Chr3126,265,569194,265,571

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)
nssv160911914.6e-005121694
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