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nsv832223

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:170,643

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 645 SVs from 75 studies. See in: genome view    
Remapped(Score: Perfect):86,134,273-86,304,915Question Mark
Overlapping variant regions from other studies: 645 SVs from 75 studies. See in: genome view    
Remapped(Score: Perfect):85,845,315-86,015,957Question Mark
Overlapping variant regions from other studies: 23 SVs from 7 studies. See in: genome view    
Submitted genomic85,522,963-85,693,605Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv832223RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1186,134,27386,304,915
nsv832223RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1185,845,31586,015,957
nsv832223Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000011.8Chr1185,522,96385,693,605

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1449370copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1449370RemappedPerfectNC_000011.10:g.(86
134273_?)_(?_86304
915)del
GRCh38.p12First PassNC_000011.10Chr1186,134,27386,304,915
nssv1449370RemappedPerfectNC_000011.9:g.(858
45315_?)_(?_860159
57)del
GRCh37.p13First PassNC_000011.9Chr1185,845,31586,015,957
nssv1449370Submitted genomicNC_000011.8:g.(855
22963_?)_(?_856936
05)del
NCBI35 (hg17)NC_000011.8Chr1185,522,96385,693,605

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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