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esv3890513

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,198

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 474 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):155,834,807-155,852,004Question Mark
Overlapping variant regions from other studies: 471 SVs from 28 studies. See in: genome view    
Submitted genomic155,064,470-155,081,667Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
esv3890513RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX155,834,807155,852,004
esv3890513Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000023.10ChrX155,064,470155,081,667

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisZygosityOther Calls in this Sample and Study
essv25753174duplicationHG00284SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,428

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
essv25753174RemappedPerfectNC_000023.11:g.155
834807_155852004du
p
GRCh38.p12First PassNC_000023.11ChrX155,834,807155,852,004
essv25753174Submitted genomicNC_000023.10:g.155
064470_155081667du
p
GRCh37 (hg19)NC_000023.10ChrX155,064,470155,081,667

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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