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nsv4382819

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:528,316

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2820 SVs from 96 studies. See in: genome view    
Remapped(Score: Good):21,972,924-22,501,239Question Mark
Overlapping variant regions from other studies: 2952 SVs from 102 studies. See in: genome view    
Submitted genomic22,441,153-22,970,223Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4382819RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1421,972,92422,501,239
nsv4382819Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000014.8Chr1422,441,15322,970,223

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15688203copy number gain210240SNP arrayGenotyping19

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15688203RemappedGoodNC_000014.9:g.(?_2
1972924)_(22501239
_?)dup
GRCh38.p12First PassNC_000014.9Chr1421,972,92422,501,239
nssv15688203Submitted genomicNC_000014.8:g.(?_2
2441153)_(22970223
_?)dup
GRCh37 (hg19)NC_000014.8Chr1422,441,15322,970,223

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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