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nsv5518289

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:87

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 100 SVs from 19 studies. See in: genome view    
Submitted genomic14,560,986-14,561,072Question Mark
Overlapping variant regions from other studies: 100 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):14,671,798-14,671,884Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5518289Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1914,560,98614,561,072
nsv5518289RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1914,671,79814,671,884

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17721711duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17721711Submitted genomicNC_000019.10:g.145
60986_14561072dup
GRCh38 (hg38)NC_000019.10Chr1914,560,98614,561,072
nssv17721711RemappedPerfectNC_000019.9:g.1467
1798_14671884dup
GRCh37.p13First PassNC_000019.9Chr1914,671,79814,671,884

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)
nssv17721711<0.00116404
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