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nsv5517695

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:168

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 173 SVs from 18 studies. See in: genome view    
Submitted genomic51,192,834-51,193,001Question Mark
Overlapping variant regions from other studies: 173 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):48,719,204-48,719,371Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5517695Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1851,192,83451,193,001
nsv5517695RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1848,719,20448,719,371

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17718154duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17718154Submitted genomicNC_000018.10:g.511
92834_51193001dup
GRCh38 (hg38)NC_000018.10Chr1851,192,83451,193,001
nssv17718154RemappedPerfectNC_000018.9:g.4871
9204_48719371dup
GRCh37.p13First PassNC_000018.9Chr1848,719,20448,719,371

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)
nssv17718154<0.00116404
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