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nsv4382839

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:107,481

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 437 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):27,640,564-27,748,044Question Mark
Overlapping variant regions from other studies: 437 SVs from 63 studies. See in: genome view    
Submitted genomic25,967,590-26,075,070Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4382839RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1727,640,56427,748,044
nsv4382839Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000017.10Chr1725,967,59026,075,070

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15622272copy number gain1-0190-002SNP arrayGenotyping23

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15622272RemappedPerfectNC_000017.11:g.(?_
27640564)_(2774804
4_?)dup
GRCh38.p12First PassNC_000017.11Chr1727,640,56427,748,044
nssv15622272Submitted genomicNC_000017.10:g.(?_
25967590)_(2607507
0_?)dup
GRCh37 (hg19)NC_000017.10Chr1725,967,59026,075,070

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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