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nsv5514153

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:79

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 89 SVs from 26 studies. See in: genome view    
Submitted genomic21,027,257-21,027,335Question Mark
Overlapping variant regions from other studies: 89 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):20,930,570-20,930,648Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5514153Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1721,027,25721,027,335
nsv5514153RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1720,930,57020,930,648

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17712134deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17712134Submitted genomicNC_000017.11:g.210
27257_21027335del
GRCh38 (hg38)NC_000017.11Chr1721,027,25721,027,335
nssv17712134RemappedPerfectNC_000017.10:g.209
30570_20930648del
GRCh37.p13First PassNC_000017.10Chr1720,930,57020,930,648

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv177121340.01636404
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