U.S. flag

An official website of the United States government

nsv4322351

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,178,860

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 5548 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):5,111,802-11,290,661Question Mark
Overlapping variant regions from other studies: 5548 SVs from 23 studies. See in: genome view    
Submitted genomic5,153,487-11,332,347Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4322351RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr35,111,80211,290,661
nsv4322351Submitted genomicGRCh37.p13Primary AssemblyNC_000003.11Chr35,153,48711,332,347

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091157inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091157RemappedPerfectNC_000003.12:g.511
1802_11290661inv
GRCh38.p12First PassNC_000003.12Chr35,111,80211,290,661
nssv16091157Submitted genomicNC_000003.11:g.515
3487_11332347inv
GRCh37.p13NC_000003.11Chr35,153,48711,332,347

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)
nssv160911574.6e-005121694
Support Center