esv2422272

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:18,657

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 53 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):96,081,345-96,100,001Question Mark
Overlapping variant regions from other studies: 53 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):95,814,509-95,833,165Question Mark
Overlapping variant regions from other studies: 5 SVs from 2 studies. See in: genome view    
Submitted genomic95,454,157-95,472,813Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2422272RemappedPerfectGRCh38Primary AssemblyFirst PassNC_000011.10Chr1196,081,34596,100,001
esv2422272RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000011.9Chr1195,814,50995,833,165
esv2422272Submitted genomicNCBI35 (hg17)NC_000011.8Chr1195,454,15795,472,813

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysis
essv5161411deletionND01496SNP arraySNP genotyping analysis

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
essv5161411RemappedPerfectNC_000011.10:g.(?_96081345)_(96100001_?)delGRCh38Primary AssemblyFirst PassNC_000011.10Chr1196,081,34596,100,001
essv5161411RemappedPerfectNC_000011.9:g.(?_95814509)_(95833165_?)delGRCh37 (hg19)Primary AssemblyFirst PassNC_000011.9Chr1195,814,50995,833,165
essv5161411Submitted genomicNC_000011.8:g.(?_95454157)_(95472813_?)delNCBI35 (hg17)NC_000011.8Chr1195,454,15795,472,813

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
essv51614112ND01496qPCROtherPass

There are no clinical assertions for this variant

There is no genotype information for this variant

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