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nsv428170

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:134,106

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 613 SVs from 67 studies. See in: genome view    
Remapped(Score: Perfect):72,318,449-72,452,554Question Mark
Overlapping variant regions from other studies: 599 SVs from 67 studies. See in: genome view    
Remapped(Score: Perfect):71,783,434-71,917,539Question Mark
Overlapping variant regions from other studies: 198 SVs from 21 studies. See in: genome view    
Submitted genomic71,421,370-71,555,475Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv428170RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr772,318,44972,452,554
nsv428170RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr771,783,43471,917,539
nsv428170Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000007.12Chr771,421,37071,555,475

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv451056copy number lossNA19189BAC aCGHProbe signal intensity94

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv451056RemappedPerfectNC_000007.14:g.(?_
72318449)_(7245255
4_?)del
GRCh38.p12First PassNC_000007.14Chr772,318,44972,452,554
nssv451056RemappedPerfectNC_000007.13:g.(?_
71783434)_(7191753
9_?)del
GRCh37.p13First PassNC_000007.13Chr771,783,43471,917,539
nssv451056Submitted genomicNC_000007.12:g.(?_
71421370)_(7155547
5_?)del
NCBI36 (hg18)NC_000007.12Chr771,421,37071,555,475

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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