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nsv4178416

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:441,867

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 408 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):53,464,148-53,906,014Question Mark
Overlapping variant regions from other studies: 409 SVs from 18 studies. See in: genome view    
Submitted genomic55,223,908-55,665,774Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4178416RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1053,464,14853,906,014
nsv4178416Submitted genomicGRCh37.p13Primary AssemblyNC_000010.10Chr1055,223,90855,665,774

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15795185deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15795185RemappedPerfectNC_000010.11:g.534
64148_53906014del
GRCh38.p12First PassNC_000010.11Chr1053,464,14853,906,014
nssv15795185Submitted genomicNC_000010.10:g.552
23908_55665774del
GRCh37.p13NC_000010.10Chr1055,223,90855,665,774

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)
nssv157951854.6e-005121694
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