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esv2941567

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 295 SVs from 52 studies. See in: genome view    
Remapped(Score: Perfect):85,514,317-85,540,317Question Mark
Overlapping variant regions from other studies: 295 SVs from 52 studies. See in: genome view    
Submitted genomic85,980,000-86,006,000Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2941567RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr185,514,31785,540,317
esv2941567Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr185,980,00086,006,000

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv7211134duplicationHuRefSequencingRead depth471,817

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv7211134RemappedPerfectNC_000001.11:g.(?_
85514317)_(8554031
7_?)dup
GRCh38.p12First PassNC_000001.11Chr185,514,31785,540,317
essv7211134Submitted genomicNC_000001.10:g.(?_
85980000)_(8600600
0_?)dup
GRCh37 (hg19)NC_000001.10Chr185,980,00086,006,000

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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