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nsv5929271

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,709

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 336 SVs from 57 studies. See in: genome view    
Submitted genomic41,054,748-41,065,456Question Mark
Overlapping variant regions from other studies: 334 SVs from 57 studies. See in: genome view    
Remapped(Score: Perfect):39,211,000-39,221,708Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5929271Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1741,054,74841,065,456
nsv5929271RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1739,211,00039,221,708

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17385410duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17385410Submitted genomicNC_000017.11:g.410
54748_41065456dup
GRCh38 (hg38)NC_000017.11Chr1741,054,74841,065,456
nssv17385410RemappedPerfectNC_000017.10:g.392
11000_39221708dup
GRCh37.p13First PassNC_000017.10Chr1739,211,00039,221,708

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)
nssv173854100.00111666
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