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esv2656438

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:8,551

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 623 SVs from 70 studies. See in: genome view    
Remapped(Score: Perfect):69,541,485-69,550,035Question Mark
Overlapping variant regions from other studies: 623 SVs from 70 studies. See in: genome view    
Remapped(Score: Perfect):67,208,721-67,217,271Question Mark
Overlapping variant regions from other studies: 325 SVs from 26 studies. See in: genome view    
Submitted genomic65,359,701-65,368,251Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2656438RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr1869,541,48569,550,035
esv2656438RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1867,208,72167,217,271
esv2656438Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000018.8Chr1865,359,70165,368,251

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
essv5395365copy number loss2354 [48]SNP arraySNP genotyping analysis112

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv5395365RemappedPerfectNC_000018.10:g.(?_
69541485)_(6955003
5_?)del
GRCh38.p12First PassNC_000018.10Chr1869,541,48569,550,035
essv5395365RemappedPerfectNC_000018.9:g.(?_6
7208721)_(67217271
_?)del
GRCh37.p13First PassNC_000018.9Chr1867,208,72167,217,271
essv5395365Submitted genomicNC_000018.8:g.(?_6
5359701)_(65368251
_?)del
NCBI36 (hg18)NC_000018.8Chr1865,359,70165,368,251

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
essv539536522354 [48]KaryotypingManual observationPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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