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esv2761451

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:156,115

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 519 SVs from 48 studies. See in: genome view    
Remapped(Score: Perfect):100,354,161-100,510,275Question Mark
Overlapping variant regions from other studies: 519 SVs from 48 studies. See in: genome view    
Remapped(Score: Perfect):101,366,389-101,522,503Question Mark
Overlapping variant regions from other studies: 114 SVs from 13 studies. See in: genome view    
Submitted genomic101,435,565-101,591,679Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2761451RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8100,354,161100,510,275
esv2761451RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8101,366,389101,522,503
esv2761451Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000008.9Chr8101,435,565101,591,679

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv6993264copy number gainSW_0507SNP arraySNP genotyping analysis34

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv6993264RemappedPerfectNC_000008.11:g.(?_
100354161)_(100510
275_?)dup
GRCh38.p12First PassNC_000008.11Chr8100,354,161100,510,275
essv6993264RemappedPerfectNC_000008.10:g.(?_
101366389)_(101522
503_?)dup
GRCh37.p13First PassNC_000008.10Chr8101,366,389101,522,503
essv6993264Submitted genomicNC_000008.9:g.(?_1
01435565)_(1015916
79_?)dup
NCBI36 (hg18)NC_000008.9Chr8101,435,565101,591,679

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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