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esv2656131

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:10,823

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 741 SVs from 71 studies. See in: genome view    
Remapped(Score: Perfect):77,545,190-77,556,012Question Mark
Overlapping variant regions from other studies: 741 SVs from 71 studies. See in: genome view    
Remapped(Score: Perfect):75,257,146-75,267,968Question Mark
Overlapping variant regions from other studies: 401 SVs from 23 studies. See in: genome view    
Submitted genomic73,386,134-73,396,956Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2656131RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr1877,545,19077,556,012
esv2656131RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1875,257,14675,267,968
esv2656131Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000018.8Chr1873,386,13473,396,956

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
essv5395460copy number loss2351 [45]SNP arraySNP genotyping analysis0essv5395255, essv5395469

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv5395460RemappedPerfectNC_000018.10:g.(?_
77545190)_(7755601
2_?)del
GRCh38.p12First PassNC_000018.10Chr1877,545,19077,556,012
essv5395460RemappedPerfectNC_000018.9:g.(?_7
5257146)_(75267968
_?)del
GRCh37.p13First PassNC_000018.9Chr1875,257,14675,267,968
essv5395460Submitted genomicNC_000018.8:g.(?_7
3386134)_(73396956
_?)del
NCBI36 (hg18)NC_000018.8Chr1873,386,13473,396,956

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
essv539546022351 [45]KaryotypingManual observationPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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