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esv3872892

  • Variant Calls:37
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,554

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 226 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):47,237,198-47,249,751Question Mark
Overlapping variant regions from other studies: 226 SVs from 46 studies. See in: genome view    
Submitted genomic47,706,401-47,718,954Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
esv3872892RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
esv3872892Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisZygosityOther Calls in this Sample and Study
essv23469316deletionHG00097SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,277
essv23469317deletionHG00127SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous2,694
essv23469318deletionHG00131SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,620
essv23469319deletionHG00150SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous2,847
essv23469320deletionHG00157SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,634
essv23469321deletionHG00181SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,659
essv23469322deletionHG00256SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,561
essv23469323deletionHG00263SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,070
essv23469324deletionHG00278SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,616
essv23469325deletionHG00331SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,283
essv23469326deletionHG00350SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,083
essv23469327deletionHG00376SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,382
essv23469328deletionHG01149SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,206
essv23469329deletionHG01325SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,518
essv23469330deletionHG01334SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,541
essv23469331deletionHG01488SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,611
essv23469332deletionHG01521SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,174
essv23469333deletionHG01556SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,843
essv23469334deletionHG01610SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,473
essv23469335deletionHG02485SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,523
essv23469336deletionHG02651SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,735
essv23469337deletionHG02792SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,723
essv23469338deletionHG03018SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,101
essv23469339deletionHG03643SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,532
essv23469340deletionHG03870SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,466
essv23469341deletionHG03928SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,278
essv23469342deletionHG04173SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,172
essv23469343deletionNA11894SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHomozygous3,394
essv23469344deletionNA19792SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,602
essv23469345deletionNA20531SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,441
essv23469346deletionNA20540SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous2,948
essv23469347deletionNA20804SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,372
essv23469348deletionNA20864SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,644
essv23469349deletionNA20910SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,061
essv23469350deletionNA21088SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,368
essv23469351deletionNA21100SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,173
essv23469352deletionNA21124SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,655

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
essv23469316RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469317RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469318RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469319RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469320RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469321RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469322RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469323RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469324RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469325RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469326RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469327RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469328RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469329RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469330RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469331RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469332RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469333RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469334RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469335RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469336RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469337RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469338RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469339RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469340RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469341RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469342RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469343RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469344RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469345RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469346RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469347RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469348RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469349RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469350RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469351RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469352RemappedPerfectNC_000014.9:g.(472
37198_47238698)_(4
7248251_47249751)d
el
GRCh38.p12First PassNC_000014.9Chr1447,238,198 (-1000, +500)47,248,751 (-500, +1000)
essv23469316Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469317Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469318Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469319Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469320Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469321Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469322Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469323Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469324Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469325Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469326Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469327Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469328Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469329Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469330Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469331Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469332Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469333Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469334Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469335Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469336Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469337Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469338Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469339Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469340Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469341Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469342Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469343Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469344Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469345Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469346Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469347Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469348Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469349Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469350Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469351Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)
essv23469352Submitted genomicNC_000014.8:g.(477
06401_47707901)_(4
7717454_47718954)d
el
GRCh37 (hg19)NC_000014.8Chr1447,707,401 (-1000, +500)47,717,954 (-500, +1000)

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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