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nsv1021906

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,983,829

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 43124 SVs from 137 studies. See in: genome view    
Remapped(Score: Perfect):178,549,208-189,533,036Question Mark
Overlapping variant regions from other studies: 43135 SVs from 137 studies. See in: genome view    
Remapped(Score: Perfect):179,470,362-190,454,190Question Mark
Overlapping variant regions from other studies: 12391 SVs from 41 studies. See in: genome view    
Submitted genomic179,707,356-190,691,184Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv1021906RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr4178,549,208189,533,036
nsv1021906RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4179,470,362190,454,190
nsv1021906Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000004.10Chr4179,707,356190,691,184

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv3445770copy number loss9862168Oligo aCGHProbe signal intensitynssv3455962, nssv3458021

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv3445770RemappedPerfectNC_000004.12:g.(?_
178549208)_(189533
036_?)del
GRCh38.p12First PassNC_000004.12Chr4178,549,208189,533,036
nssv3445770RemappedPerfectNC_000004.11:g.(?_
179470362)_(190454
190_?)del
GRCh37.p13First PassNC_000004.11Chr4179,470,362190,454,190
nssv3445770Submitted genomicNC_000004.10:g.(?_
179707356)_(190691
184_?)del
NCBI36 (hg18)NC_000004.10Chr4179,707,356190,691,184

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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