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nsv830396

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:221,882

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 471 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):91,825,538-92,047,419Question Mark
Overlapping variant regions from other studies: 471 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):91,121,355-91,343,236Question Mark
Overlapping variant regions from other studies: 46 SVs from 5 studies. See in: genome view    
Submitted genomic91,157,111-91,378,992Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv830396RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr591,825,53892,047,419
nsv830396RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr591,121,35591,343,236
nsv830396Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000005.8Chr591,157,11191,378,992

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1444846copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1444846RemappedPerfectNC_000005.10:g.(91
825538_?)_(?_92047
419)del
GRCh38.p12First PassNC_000005.10Chr591,825,53892,047,419
nssv1444846RemappedPerfectNC_000005.9:g.(911
21355_?)_(?_913432
36)del
GRCh37.p13First PassNC_000005.9Chr591,121,35591,343,236
nssv1444846Submitted genomicNC_000005.8:g.(911
57111_?)_(?_913789
92)del
NCBI35 (hg17)NC_000005.8Chr591,157,11191,378,992

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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