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nsv5521170

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:116,352

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1659 SVs from 103 studies. See in: genome view    
Submitted genomic54,220,538-54,336,889Question Mark
Overlapping variant regions from other studies: 246 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):194,905-311,256Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5521170Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1954,220,53854,336,889
nsv5521170RemappedPerfectGRCh37.p13PATCHESFirst PassNW_004166865.1Chr19|NW_0
04166865.1
194,905311,256

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17725506duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17725506Submitted genomicNC_000019.10:g.542
20538_54336889dup
GRCh38 (hg38)NC_000019.10Chr1954,220,53854,336,889
nssv17725506RemappedPerfectNW_004166865.1:g.1
94905_311256dup
GRCh37.p13First PassNW_004166865.1Chr19|NW_0
04166865.1
194,905311,256

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)
nssv17725506<0.00116404
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