U.S. flag

An official website of the United States government

nsv471376

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:47,848

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1130 SVs from 75 studies. See in: genome view    
Remapped(Score: Perfect):22,869,466-22,917,313Question Mark
Overlapping variant regions from other studies: 1431 SVs from 78 studies. See in: genome view    
Remapped(Score: Perfect):22,955,755-23,003,602Question Mark
Overlapping variant regions from other studies: 59 SVs from 11 studies. See in: genome view    
Submitted genomic20,507,196-20,555,043Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv471376RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000015.10Chr1522,869,46622,917,313
nsv471376RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1522,955,75523,003,602
nsv471376Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000015.8Chr1520,507,19620,555,043

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
nssv548106copy number lossNA18507SequencingRead depth1208

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv548106RemappedPerfectNC_000015.10:g.(22
869466_?)_(?_22917
313)del
GRCh38.p12First PassNC_000015.10Chr1522,869,46622,917,313
nssv548106RemappedPerfectNC_000015.9:g.(229
55755_?)_(?_230036
02)del
GRCh37.p13First PassNC_000015.9Chr1522,955,75523,003,602
nssv548106Submitted genomicNC_000015.8:g.(205
07196_?)_(?_205550
43)del
NCBI35 (hg17)NC_000015.8Chr1520,507,19620,555,043

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
nssv5481064NA18507Oligo aCGHProbe signal intensityPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

Support Center