nsv483009

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:177,418

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 524 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):42,829,470-43,006,887Question Mark
Overlapping variant regions from other studies: 517 SVs from 36 studies. See in: genome view    
Submitted genomic40,981,487-41,158,904Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv483009RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000017.11Chr1742,829,47043,006,887
nsv483009Submitted genomicGRCh37 (hg19)NC_000017.10Chr1740,981,48741,158,904

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv2996410copy number gainBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nssv2996410RemappedPerfectNC_000017.11:g.(?_
42829470)_(4300688
7_?)dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000017.11Chr1742,829,47043,006,887
nssv2996410Submitted genomicNC_000017.10:g.(?_
40981487)_(4115890
4_?)dup
GRCh37 (hg19)NC_000017.10Chr1740,981,48741,158,904

Validation Information

Variant Call IDExperiment IDMethodAnalysisResult
nssv29964102FISHProbe signal intensityPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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