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nsv5521569

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:311

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 143 SVs from 28 studies. See in: genome view    
Submitted genomic33,747,333-33,747,643Question Mark
Overlapping variant regions from other studies: 143 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):32,335,139-32,335,449Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5521569Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2033,747,33333,747,643
nsv5521569RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2032,335,13932,335,449

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17732046deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17732046Submitted genomicNC_000020.11:g.337
47333_33747643del
GRCh38 (hg38)NC_000020.11Chr2033,747,33333,747,643
nssv17732046RemappedPerfectNC_000020.10:g.323
35139_32335449del
GRCh37.p13First PassNC_000020.10Chr2032,335,13932,335,449

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)
nssv177320460.0734676404
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