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nsv4327115

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:30,351,674

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 19224 SVs from 24 studies. See in: genome view    
Remapped(Score: Good):132,163,857-162,515,530Question Mark
Overlapping variant regions from other studies: 19213 SVs from 24 studies. See in: genome view    
Submitted genomic131,882,701-162,233,318Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4327115RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3132,163,857162,515,530
nsv4327115Submitted genomicGRCh37.p13Primary AssemblyNC_000003.11Chr3131,882,701162,233,318

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091197inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091197RemappedGoodNC_000003.12:g.132
163857_162515530in
v
GRCh38.p12First PassNC_000003.12Chr3132,163,857162,515,530
nssv16091197Submitted genomicNC_000003.11:g.131
882701_162233318in
v
GRCh37.p13NC_000003.11Chr3131,882,701162,233,318

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)
nssv160911974.6e-005121694
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