nsv824627

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,363

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 147 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):50,312,425-50,315,787Question Mark
Overlapping variant regions from other studies: 147 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):51,224,985-51,228,347Question Mark
Overlapping variant regions from other studies: 81 SVs from 19 studies. See in: genome view    
Submitted genomic51,387,538-51,390,900Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv824627RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000008.11Chr850,312,42550,315,787
nsv824627RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000008.10Chr851,224,98551,228,347
nsv824627Submitted genomicNCBI36 (hg18)NC_000008.9Chr851,387,53851,390,900

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1434531copy number lossNA18570Oligo aCGHProbe signal intensity629

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nssv1434531RemappedPerfectNC_000008.11:g.(?_
50312425)_(5031578
7_?)del
GRCh38 (hg38)Primary AssemblyFirst PassNC_000008.11Chr850,312,42550,315,787
nssv1434531RemappedPerfectNC_000008.10:g.(?_
51224985)_(5122834
7_?)del
GRCh37 (hg19)Primary AssemblyFirst PassNC_000008.10Chr851,224,98551,228,347
nssv1434531Submitted genomicNC_000008.9:g.(?_5
1387538)_(51390900
_?)del
NCBI36 (hg18)NC_000008.9Chr851,387,53851,390,900

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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