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esv3586622

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,734

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 129 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):81,887,909-81,892,642Question Mark
Overlapping variant regions from other studies: 129 SVs from 25 studies. See in: genome view    
Submitted genomic82,353,594-82,358,327Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
esv3586622RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr181,887,90981,892,642
esv3586622Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr182,353,59482,358,327

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisZygosityOther Calls in this Sample and Study
essv9993532duplicationSAMN01091010SequencingRead depth and paired-end mappingHeterozygous2,708
essv9993533duplicationSAMN01090999SequencingRead depth and paired-end mappingHeterozygous2,741

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
essv9993532RemappedPerfectNC_000001.11:g.818
87909_81892642dup
GRCh38.p12First PassNC_000001.11Chr181,887,90981,892,642
essv9993533RemappedPerfectNC_000001.11:g.818
87909_81892642dup
GRCh38.p12First PassNC_000001.11Chr181,887,90981,892,642
essv9993532Submitted genomicNC_000001.10:g.823
53594_82358327dup
GRCh37 (hg19)NC_000001.10Chr182,353,59482,358,327
essv9993533Submitted genomicNC_000001.10:g.823
53594_82358327dup
GRCh37 (hg19)NC_000001.10Chr182,353,59482,358,327

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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