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nsv5523121

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:604

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 98 SVs from 21 studies. See in: genome view    
Submitted genomic29,087,743-29,088,346Question Mark
Overlapping variant regions from other studies: 98 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):27,414,761-27,415,364Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5523121Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1729,087,74329,088,346
nsv5523121RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1727,414,76127,415,364

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17712402deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17712402Submitted genomicNC_000017.11:g.290
87743_29088346del
GRCh38 (hg38)NC_000017.11Chr1729,087,74329,088,346
nssv17712402RemappedPerfectNC_000017.10:g.274
14761_27415364del
GRCh37.p13First PassNC_000017.10Chr1727,414,76127,415,364

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)
nssv177124020.002106404
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