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nsv4210412

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:354,807

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 292 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):46,451,248-46,806,054Question Mark
Overlapping variant regions from other studies: 292 SVs from 20 studies. See in: genome view    
Submitted genomic46,472,798-46,827,604Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4210412RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1146,451,24846,806,054
nsv4210412Submitted genomicGRCh37.p13Primary AssemblyNC_000011.9Chr1146,472,79846,827,604

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15950340duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15950340RemappedPerfectNC_000011.10:g.464
51248_46806054dup
GRCh38.p12First PassNC_000011.10Chr1146,451,24846,806,054
nssv15950340Submitted genomicNC_000011.9:g.4647
2798_46827604dup
GRCh37.p13NC_000011.9Chr1146,472,79846,827,604

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)
nssv159503404.6e-005121694
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