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nsv4196538

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,650

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 50 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):4,990,161-4,998,810Question Mark
Overlapping variant regions from other studies: 50 SVs from 6 studies. See in: genome view    
Submitted genomic5,011,391-5,020,040Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4196538RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr114,990,1614,998,810
nsv4196538Submitted genomicGRCh37.p13Primary AssemblyNC_000011.9Chr115,011,3915,020,040

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15952850duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15952850RemappedPerfectNC_000011.10:g.499
0161_4998810dup
GRCh38.p12First PassNC_000011.10Chr114,990,1614,998,810
nssv15952850Submitted genomicNC_000011.9:g.5011
391_5020040dup
GRCh37.p13NC_000011.9Chr115,011,3915,020,040

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)
nssv159528504.6e-005121694
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