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nsv469894

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:187,705

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1253 SVs from 78 studies. See in: genome view    
Remapped(Score: Perfect):26,558,113-26,745,817Question Mark
Overlapping variant regions from other studies: 1253 SVs from 78 studies. See in: genome view    
Remapped(Score: Perfect):26,803,260-26,990,964Question Mark
Overlapping variant regions from other studies: 1 SVs from 1 studies. See in: genome view    
Submitted genomic24,350,621-24,538,325Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv469894RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000015.10Chr1526,558,11326,745,817
nsv469894RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1526,803,26026,990,964
nsv469894Submitted genomicNCBI34 (hg16)Primary AssemblyNC_000015.7Chr1524,350,62124,538,325

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1675788copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv1675788RemappedPerfectNC_000015.10:g.(?_
26558113)_(2674581
7_?)del
GRCh38.p12First PassNC_000015.10Chr1526,558,11326,745,817
nssv1675788RemappedPerfectNC_000015.9:g.(?_2
6803260)_(26990964
_?)del
GRCh37.p13First PassNC_000015.9Chr1526,803,26026,990,964
nssv1675788Submitted genomicNC_000015.7:g.(?_2
4350621)_(24538325
_?)del
NCBI34 (hg16)NC_000015.7Chr1524,350,62124,538,325

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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