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nsv833371

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:211,448

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 624 SVs from 61 studies. See in: genome view    
Remapped(Score: Perfect):11,288,681-11,500,128Question Mark
Overlapping variant regions from other studies: 624 SVs from 61 studies. See in: genome view    
Remapped(Score: Perfect):11,191,998-11,403,445Question Mark
Overlapping variant regions from other studies: 33 SVs from 9 studies. See in: genome view    
Submitted genomic11,132,723-11,344,170Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv833371RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1711,288,68111,500,128
nsv833371RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1711,191,99811,403,445
nsv833371Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000017.9Chr1711,132,72311,344,170

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1453122copy number gainBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1453122RemappedPerfectNC_000017.11:g.(11
288681_?)_(?_11500
128)dup
GRCh38.p12First PassNC_000017.11Chr1711,288,68111,500,128
nssv1453122RemappedPerfectNC_000017.10:g.(11
191998_?)_(?_11403
445)dup
GRCh37.p13First PassNC_000017.10Chr1711,191,99811,403,445
nssv1453122Submitted genomicNC_000017.9:g.(111
32723_?)_(?_113441
70)dup
NCBI35 (hg17)NC_000017.9Chr1711,132,72311,344,170

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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