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nsv5522128

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:164

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 125 SVs from 29 studies. See in: genome view    
Submitted genomic53,880,983-53,881,146Question Mark
Overlapping variant regions from other studies: 124 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):54,384,237-54,384,400Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5522128Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1953,880,98353,881,146
nsv5522128RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1954,384,23754,384,400

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17724318duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17724318Submitted genomicNC_000019.10:g.538
80983_53881146dup
GRCh38 (hg38)NC_000019.10Chr1953,880,98353,881,146
nssv17724318RemappedPerfectNC_000019.9:g.5438
4237_54384400dup
GRCh37.p13First PassNC_000019.9Chr1954,384,23754,384,400

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)
nssv17724318<0.00126404
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