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nsv6621755

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:133,507

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 703 SVs from 76 studies. See in: genome view    
Remapped(Score: Perfect):8,223,474-8,356,980Question Mark
Overlapping variant regions from other studies: 703 SVs from 76 studies. See in: genome view    
Submitted genomic8,376,070-8,509,576Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv6621755RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr128,223,4748,356,980
nsv6621755Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr128,376,0708,509,576

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv18297804duplicationOSC5011SNP arrayProbe signal intensity9

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv18297804RemappedPerfectNC_000012.12:g.(?_
8223474)_(8356980_
?)dup
GRCh38.p12First PassNC_000012.12Chr128,223,4748,356,980
nssv18297804Submitted genomicNC_000012.11:g.(?_
8376070)_(8509576_
?)dup
GRCh37 (hg19)NC_000012.11Chr128,376,0708,509,576

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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