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nsv471377

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:29,060

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1092 SVs from 71 studies. See in: genome view    
Remapped(Score: Perfect):22,838,660-22,867,719Question Mark
Overlapping variant regions from other studies: 1393 SVs from 74 studies. See in: genome view    
Remapped(Score: Perfect):23,005,349-23,034,408Question Mark
Overlapping variant regions from other studies: 57 SVs from 11 studies. See in: genome view    
Submitted genomic20,556,790-20,585,849Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv471377RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000015.10Chr1522,838,66022,867,719
nsv471377RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1523,005,34923,034,408
nsv471377Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000015.8Chr1520,556,79020,585,849

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
nssv548107copy number lossNA18507SequencingRead depth1208

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv548107RemappedPerfectNC_000015.10:g.(22
838660_?)_(?_22867
719)del
GRCh38.p12First PassNC_000015.10Chr1522,838,66022,867,719
nssv548107RemappedPerfectNC_000015.9:g.(230
05349_?)_(?_230344
08)del
GRCh37.p13First PassNC_000015.9Chr1523,005,34923,034,408
nssv548107Submitted genomicNC_000015.8:g.(205
56790_?)_(?_205858
49)del
NCBI35 (hg17)NC_000015.8Chr1520,556,79020,585,849

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
nssv5481074NA18507Oligo aCGHProbe signal intensityPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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