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nsv829835

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:206,654

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1451 SVs from 83 studies. See in: genome view    
Remapped(Score: Perfect):1,103,798-1,310,451Question Mark
Overlapping variant regions from other studies: 1451 SVs from 83 studies. See in: genome view    
Remapped(Score: Perfect):1,097,586-1,304,239Question Mark
Overlapping variant regions from other studies: 57 SVs from 7 studies. See in: genome view    
Submitted genomic1,087,416-1,294,069Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv829835RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr41,103,7981,310,451
nsv829835RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr41,097,5861,304,239
nsv829835Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000004.9Chr41,087,4161,294,069

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1443327copy number gainBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1443327RemappedPerfectNC_000004.12:g.(11
03798_?)_(?_131045
1)dup
GRCh38.p12First PassNC_000004.12Chr41,103,7981,310,451
nssv1443327RemappedPerfectNC_000004.11:g.(10
97586_?)_(?_130423
9)dup
GRCh37.p13First PassNC_000004.11Chr41,097,5861,304,239
nssv1443327Submitted genomicNC_000004.9:g.(108
7416_?)_(?_1294069
)dup
NCBI35 (hg17)NC_000004.9Chr41,087,4161,294,069

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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