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esv3827587

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:97,180

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 382 SVs from 53 studies. See in: genome view    
Remapped(Score: Perfect):193,123,855-193,222,034Question Mark
Overlapping variant regions from other studies: 382 SVs from 53 studies. See in: genome view    
Submitted genomic193,988,581-194,086,760Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
esv3827587RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2193,124,355 (-500, +0)193,221,534 (-0, +500)
esv3827587Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2193,989,081 (-500, +0)194,086,260 (-0, +500)

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisZygosityOther Calls in this Sample and Study
essv18026943deletionHG00542SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,469

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
essv18026943RemappedPerfectNC_000002.12:g.(19
3123855_193124355)
_(193221534_193222
034)del
GRCh38.p12First PassNC_000002.12Chr2193,124,355 (-500, +0)193,221,534 (-0, +500)
essv18026943Submitted genomicNC_000002.11:g.(19
3988581_193989081)
_(194086260_194086
760)del
GRCh37 (hg19)NC_000002.11Chr2193,989,081 (-500, +0)194,086,260 (-0, +500)

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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