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nsv3125747

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:507,148

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1249 SVs from 72 studies. See in: genome view    
Remapped(Score: Perfect):204,686,178-205,193,325Question Mark
Overlapping variant regions from other studies: 1250 SVs from 72 studies. See in: genome view    
Submitted genomic205,550,901-206,058,049Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv3125747RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2204,686,178205,193,325
nsv3125747Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2205,550,901206,058,049

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv14143142copy number lossSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv14143142RemappedPerfectNC_000002.12:g.(?_
204686178)_(205193
325_?)del
GRCh38.p12First PassNC_000002.12Chr2204,686,178205,193,325
nssv14143142Submitted genomicNC_000002.11:g.(?_
205550901)_(206058
049_?)del
GRCh37 (hg19)NC_000002.11Chr2205,550,901206,058,049

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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