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nsv5532198

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:605

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 107 SVs from 28 studies. See in: genome view    
Submitted genomic54,711,752-54,712,356Question Mark
Overlapping variant regions from other studies: 41 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):686,119-686,723Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5532198Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1954,711,75254,712,356
nsv5532198RemappedPerfectGRCh37.p13PATCHESFirst PassNW_004166865.1Chr19|NW_0
04166865.1
686,119686,723

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17725558deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17725558Submitted genomicNC_000019.10:g.547
11752_54712356del
GRCh38 (hg38)NC_000019.10Chr1954,711,75254,712,356
nssv17725558RemappedPerfectNW_004166865.1:g.6
86119_686723del
GRCh37.p13First PassNW_004166865.1Chr19|NW_0
04166865.1
686,119686,723

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)
nssv177255580.16510596404
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