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nsv4378321

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:48,992

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1131 SVs from 96 studies. See in: genome view    
Remapped(Score: Perfect):196,858,712-196,907,703Question Mark
Overlapping variant regions from other studies: 1131 SVs from 96 studies. See in: genome view    
Submitted genomic196,827,842-196,876,833Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4378321RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1196,858,712196,907,703
nsv4378321Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1196,827,842196,876,833

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15650740copy number gain2-1363-003SNP arrayGenotyping26

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15650740RemappedPerfectNC_000001.11:g.(?_
196858712)_(196907
703_?)dup
GRCh38.p12First PassNC_000001.11Chr1196,858,712196,907,703
nssv15650740Submitted genomicNC_000001.10:g.(?_
196827842)_(196876
833_?)dup
GRCh37 (hg19)NC_000001.10Chr1196,827,842196,876,833

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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