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nsv821672

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,030,675

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 3159 SVs from 95 studies. See in: genome view    
Remapped(Score: Perfect):64,584,661-65,615,335Question Mark
Overlapping variant regions from other studies: 3159 SVs from 95 studies. See in: genome view    
Remapped(Score: Perfect):65,158,793-66,189,467Question Mark
Overlapping variant regions from other studies: 99 SVs from 11 studies. See in: genome view    
Submitted genomic64,056,794-65,087,468Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv821672RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1364,584,66165,615,335
nsv821672RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1365,158,79366,189,467
nsv821672Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000013.9Chr1364,056,79465,087,468

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1421247copy number lossROMAProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv1421247RemappedPerfectNC_000013.11:g.(?_
64584661)_(6561533
5_?)del
GRCh38.p12First PassNC_000013.11Chr1364,584,66165,615,335
nssv1421247RemappedPerfectNC_000013.10:g.(?_
65158793)_(6618946
7_?)del
GRCh37.p13First PassNC_000013.10Chr1365,158,79366,189,467
nssv1421247Submitted genomicNC_000013.9:g.(?_6
4056794)_(65087468
_?)del
NCBI35 (hg17)NC_000013.9Chr1364,056,79465,087,468

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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