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nsv5519218

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:139

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 91 SVs from 17 studies. See in: genome view    
Submitted genomic28,725,346-28,725,484Question Mark
Overlapping variant regions from other studies: 91 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):27,052,364-27,052,502Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5519218Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1728,725,34628,725,484
nsv5519218RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1727,052,36427,052,502

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17712376duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17712376Submitted genomicNC_000017.11:g.287
25346_28725484dup
GRCh38 (hg38)NC_000017.11Chr1728,725,34628,725,484
nssv17712376RemappedPerfectNC_000017.10:g.270
52364_27052502dup
GRCh37.p13First PassNC_000017.10Chr1727,052,36427,052,502

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)
nssv17712376<0.00116404
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