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nsv833901

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:237,772

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 691 SVs from 71 studies. See in: genome view    
Remapped(Score: Perfect):4,243,165-4,480,936Question Mark
Overlapping variant regions from other studies: 691 SVs from 71 studies. See in: genome view    
Remapped(Score: Perfect):4,223,812-4,461,583Question Mark
Overlapping variant regions from other studies: 93 SVs from 7 studies. See in: genome view    
Submitted genomic4,171,812-4,409,583Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv833901RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr204,243,1654,480,936
nsv833901RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr204,223,8124,461,583
nsv833901Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000020.9Chr204,171,8124,409,583

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1454906copy number gainBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1454906RemappedPerfectNC_000020.11:g.(42
43165_?)_(?_448093
6)dup
GRCh38.p12First PassNC_000020.11Chr204,243,1654,480,936
nssv1454906RemappedPerfectNC_000020.10:g.(42
23812_?)_(?_446158
3)dup
GRCh37.p13First PassNC_000020.10Chr204,223,8124,461,583
nssv1454906Submitted genomicNC_000020.9:g.(417
1812_?)_(?_4409583
)dup
NCBI35 (hg17)NC_000020.9Chr204,171,8124,409,583

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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