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nsv4387140

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:287,420

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 640 SVs from 62 studies. See in: genome view    
Remapped(Score: Perfect):59,260,424-59,547,843Question Mark
Overlapping variant regions from other studies: 640 SVs from 62 studies. See in: genome view    
Submitted genomic59,027,897-59,315,316Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4387140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1159,260,42459,547,843
nsv4387140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1159,027,89759,315,316

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15632935copy number gain10-1076-004SNP arrayGenotyping20

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15632935RemappedPerfectNC_000011.10:g.(?_
59260424)_(5954784
3_?)dup
GRCh38.p12First PassNC_000011.10Chr1159,260,42459,547,843
nssv15632935Submitted genomicNC_000011.9:g.(?_5
9027897)_(59315316
_?)dup
GRCh37 (hg19)NC_000011.9Chr1159,027,89759,315,316

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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