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nsv1036409

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:500,513

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 4256 SVs from 95 studies. See in: genome view    
Remapped(Score: Good):22,007,752-22,508,264Question Mark
Overlapping variant regions from other studies: 4393 SVs from 101 studies. See in: genome view    
Remapped(Score: Perfect):22,475,991-22,977,249Question Mark
Overlapping variant regions from other studies: 1066 SVs from 29 studies. See in: genome view    
Submitted genomic21,545,831-22,047,089Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv1036409RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1422,007,75222,508,264
nsv1036409RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1422,475,99122,977,249
nsv1036409Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000014.7Chr1421,545,83122,047,089

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv3532171copy number lossSNP arrayProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv3532171RemappedGoodNC_000014.9:g.(?_2
2007752)_(22508264
_?)del
GRCh38.p12First PassNC_000014.9Chr1422,007,75222,508,264
nssv3532171RemappedPerfectNC_000014.8:g.(?_2
2475991)_(22977249
_?)del
GRCh37.p13First PassNC_000014.8Chr1422,475,99122,977,249
nssv3532171Submitted genomicNC_000014.7:g.(?_2
1545831)_(22047089
_?)del
NCBI36 (hg18)NC_000014.7Chr1421,545,83122,047,089

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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