nsv829775

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:194,785

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 434 SVs from 53 studies. See in: genome view    
Remapped(Score: Perfect):162,493,830-162,688,614Question Mark
Overlapping variant regions from other studies: 434 SVs from 53 studies. See in: genome view    
Remapped(Score: Perfect):162,211,618-162,406,402Question Mark
Overlapping variant regions from other studies: 51 SVs from 9 studies. See in: genome view    
Submitted genomic163,694,320-163,889,104Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv829775RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000003.12Chr3162,493,830162,688,614
nsv829775RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000003.11Chr3162,211,618162,406,402
nsv829775Submitted genomicNCBI35 (hg17)NC_000003.9Chr3163,694,320163,889,104

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1443143copy number gainBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nssv1443143RemappedPerfectNC_000003.12:g.(16
2493830_?)_(?_1626
88614)dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000003.12Chr3162,493,830162,688,614
nssv1443143RemappedPerfectNC_000003.11:g.(16
2211618_?)_(?_1624
06402)dup
GRCh37 (hg19)Primary AssemblyFirst PassNC_000003.11Chr3162,211,618162,406,402
nssv1443143Submitted genomicNC_000003.9:g.(163
694320_?)_(?_16388
9104)dup
NCBI35 (hg17)NC_000003.9Chr3163,694,320163,889,104

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