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nsv833238

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:225,472

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 543 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):54,562,233-54,787,704Question Mark
Overlapping variant regions from other studies: 543 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):54,596,145-54,821,616Question Mark
Overlapping variant regions from other studies: 42 SVs from 5 studies. See in: genome view    
Submitted genomic53,153,646-53,379,117Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv833238RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1654,562,23354,787,704
nsv833238RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1654,596,14554,821,616
nsv833238Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000016.8Chr1653,153,64653,379,117

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1452750copy number gainBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1452750RemappedPerfectNC_000016.10:g.(54
562233_?)_(?_54787
704)dup
GRCh38.p12First PassNC_000016.10Chr1654,562,23354,787,704
nssv1452750RemappedPerfectNC_000016.9:g.(545
96145_?)_(?_548216
16)dup
GRCh37.p13First PassNC_000016.9Chr1654,596,14554,821,616
nssv1452750Submitted genomicNC_000016.8:g.(531
53646_?)_(?_533791
17)dup
NCBI35 (hg17)NC_000016.8Chr1653,153,64653,379,117

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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