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nsv4317801

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,315,818

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 10367 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):106,441,422-123,757,239Question Mark
Overlapping variant regions from other studies: 10367 SVs from 24 studies. See in: genome view    
Submitted genomic106,160,269-123,476,086Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4317801RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3106,441,422123,757,239
nsv4317801Submitted genomicGRCh37.p13Primary AssemblyNC_000003.11Chr3106,160,269123,476,086

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091184inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091184RemappedPerfectNC_000003.12:g.106
441422_123757239in
v
GRCh38.p12First PassNC_000003.12Chr3106,441,422123,757,239
nssv16091184Submitted genomicNC_000003.11:g.106
160269_123476086in
v
GRCh37.p13NC_000003.11Chr3106,160,269123,476,086

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)
nssv160911844.6e-005121694
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