U.S. flag

An official website of the United States government

esv2656343

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:2,117

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 608 SVs from 69 studies. See in: genome view    
Remapped(Score: Perfect):66,099,714-66,101,830Question Mark
Overlapping variant regions from other studies: 608 SVs from 69 studies. See in: genome view    
Remapped(Score: Perfect):63,766,950-63,769,066Question Mark
Overlapping variant regions from other studies: 350 SVs from 27 studies. See in: genome view    
Submitted genomic61,917,930-61,920,046Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2656343RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr1866,099,71466,101,830
esv2656343RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1863,766,95063,769,066
esv2656343Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000018.8Chr1861,917,93061,920,046

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
essv5395159copy number gain2243 [60]SNP arraySNP genotyping analysis36

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv5395159RemappedPerfectNC_000018.10:g.(?_
66099714)_(6610183
0_?)dup
GRCh38.p12First PassNC_000018.10Chr1866,099,71466,101,830
essv5395159RemappedPerfectNC_000018.9:g.(?_6
3766950)_(63769066
_?)dup
GRCh37.p13First PassNC_000018.9Chr1863,766,95063,769,066
essv5395159Submitted genomicNC_000018.8:g.(?_6
1917930)_(61920046
_?)dup
NCBI36 (hg18)NC_000018.8Chr1861,917,93061,920,046

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
essv539515922243 [60]KaryotypingManual observationPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

Support Center