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nsv4181465

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:81,879

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 50 SVs from 10 studies. See in: genome view    
Remapped(Score: Perfect):70,082,132-70,164,010Question Mark
Overlapping variant regions from other studies: 50 SVs from 10 studies. See in: genome view    
Submitted genomic71,841,888-71,923,766Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4181465RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1070,082,13270,164,010
nsv4181465Submitted genomicGRCh37.p13Primary AssemblyNC_000010.10Chr1071,841,88871,923,766

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15951431duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15951431RemappedPerfectNC_000010.11:g.700
82132_70164010dup
GRCh38.p12First PassNC_000010.11Chr1070,082,13270,164,010
nssv15951431Submitted genomicNC_000010.10:g.718
41888_71923766dup
GRCh37.p13NC_000010.10Chr1071,841,88871,923,766

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)
nssv159514314.6e-005121694
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