nsv469523

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:102,621

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 383 SVs from 58 studies. See in: genome view    
Remapped(Score: Perfect):34,042,032-34,144,652Question Mark
Overlapping variant regions from other studies: 383 SVs from 58 studies. See in: genome view    
Remapped(Score: Perfect):34,194,967-34,297,587Question Mark
Overlapping variant regions from other studies: 1 SVs from 1 studies. See in: genome view    
Submitted genomic34,086,234-34,188,854Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv469523RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000012.12Chr1234,042,03234,144,652
nsv469523RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000012.11Chr1234,194,96734,297,587
nsv469523Submitted genomicNCBI34 (hg16)NC_000012.8Chr1234,086,23434,188,854

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1674864copy number gainBAC aCGHProbe signal intensity
nssv1675309copy number gainBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nssv1674864RemappedPerfectNC_000012.12:g.(?_
34042032)_(3414465
2_?)dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000012.12Chr1234,042,03234,144,652
nssv1675309RemappedPerfectNC_000012.12:g.(?_
34042032)_(3414465
2_?)dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000012.12Chr1234,042,03234,144,652
nssv1674864RemappedPerfectNC_000012.11:g.(?_
34194967)_(3429758
7_?)dup
GRCh37 (hg19)Primary AssemblyFirst PassNC_000012.11Chr1234,194,96734,297,587
nssv1675309RemappedPerfectNC_000012.11:g.(?_
34194967)_(3429758
7_?)dup
GRCh37 (hg19)Primary AssemblyFirst PassNC_000012.11Chr1234,194,96734,297,587
nssv1674864Submitted genomicNC_000012.8:g.(?_3
4086234)_(34188854
_?)dup
NCBI34 (hg16)NC_000012.8Chr1234,086,23434,188,854
nssv1675309Submitted genomicNC_000012.8:g.(?_3
4086234)_(34188854
_?)dup
NCBI34 (hg16)NC_000012.8Chr1234,086,23434,188,854

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

Support Center