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nsv4237808

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:946,503

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1518 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):1,582,120-2,528,622Question Mark
Overlapping variant regions from other studies: 1518 SVs from 20 studies. See in: genome view    
Submitted genomic1,485,414-2,431,916Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4237808RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr171,582,1202,528,622
nsv4237808Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr171,485,4142,431,916

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15958586duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15958586RemappedPerfectNC_000017.11:g.158
2120_2528622dup
GRCh38.p12First PassNC_000017.11Chr171,582,1202,528,622
nssv15958586Submitted genomicNC_000017.10:g.148
5414_2431916dup
GRCh37.p13NC_000017.10Chr171,485,4142,431,916

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)
nssv159585864.6e-005121694
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