nsv824629

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,711

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 89 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):51,747,643-51,749,353Question Mark
Overlapping variant regions from other studies: 89 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):52,660,203-52,661,913Question Mark
Overlapping variant regions from other studies: 37 SVs from 11 studies. See in: genome view    
Submitted genomic52,822,756-52,824,466Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv824629RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000008.11Chr851,747,64351,749,353
nsv824629RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000008.10Chr852,660,20352,661,913
nsv824629Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000008.9Chr852,822,75652,824,466

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1426817copy number lossAK6Oligo aCGHProbe signal intensity714

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv1426817RemappedPerfectNC_000008.11:g.(?_
51747643)_(5174935
3_?)del
GRCh38 (hg38)First PassNC_000008.11Chr851,747,64351,749,353
nssv1426817RemappedPerfectNC_000008.10:g.(?_
52660203)_(5266191
3_?)del
GRCh37 (hg19)First PassNC_000008.10Chr852,660,20352,661,913
nssv1426817Submitted genomicNC_000008.9:g.(?_5
2822756)_(52824466
_?)del
NCBI36 (hg18)NC_000008.9Chr852,822,75652,824,466

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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