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nsv5548097

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:98

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 105 SVs from 26 studies. See in: genome view    
Submitted genomic30,623,673-30,623,770Question Mark
Overlapping variant regions from other studies: 105 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):31,019,660-31,019,757Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5548097Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2230,623,67330,623,770
nsv5548097RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2231,019,66031,019,757

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17728432duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17728432Submitted genomicNC_000022.11:g.306
23673_30623770dup
GRCh38 (hg38)NC_000022.11Chr2230,623,67330,623,770
nssv17728432RemappedPerfectNC_000022.10:g.310
19660_31019757dup
GRCh37.p13First PassNC_000022.10Chr2231,019,66031,019,757

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)
nssv17728432<0.00126404
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