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nsv4176852

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:133,412

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 178 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):96,605,068-96,738,479Question Mark
Overlapping variant regions from other studies: 178 SVs from 19 studies. See in: genome view    
Submitted genomic99,367,350-99,500,761Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4176852RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr996,605,06896,738,479
nsv4176852Submitted genomicGRCh37.p13Primary AssemblyNC_000009.11Chr999,367,35099,500,761

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15985945duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15985945RemappedPerfectNC_000009.12:g.966
05068_96738479dup
GRCh38.p12First PassNC_000009.12Chr996,605,06896,738,479
nssv15985945Submitted genomicNC_000009.11:g.993
67350_99500761dup
GRCh37.p13NC_000009.11Chr999,367,35099,500,761

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)
nssv159859454.6e-005121694
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