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nsv4076908

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:562,972

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 406 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):19,601,002-20,163,973Question Mark
Overlapping variant regions from other studies: 406 SVs from 17 studies. See in: genome view    
Submitted genomic19,642,494-20,205,465Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4076908RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr319,601,00220,163,973
nsv4076908Submitted genomicGRCh37.p13Primary AssemblyNC_000003.11Chr319,642,49420,205,465

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15972374duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15972374RemappedPerfectNC_000003.12:g.196
01002_20163973dup
GRCh38.p12First PassNC_000003.12Chr319,601,00220,163,973
nssv15972374Submitted genomicNC_000003.11:g.196
42494_20205465dup
GRCh37.p13NC_000003.11Chr319,642,49420,205,465

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)
nssv159723744.6e-005121692
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