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nsv5416860

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:125

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 209 SVs from 46 studies. See in: genome view    
Submitted genomic25,359,005-25,359,129Question Mark
Overlapping variant regions from other studies: 209 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):25,685,496-25,685,620Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5416860Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr125,359,00525,359,129
nsv5416860RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr125,685,49625,685,620

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16900205duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16900205Submitted genomicNC_000001.11:g.253
59005_25359129dup
GRCh38 (hg38)NC_000001.11Chr125,359,00525,359,129
nssv16900205RemappedPerfectNC_000001.10:g.256
85496_25685620dup
GRCh37.p13First PassNC_000001.10Chr125,685,49625,685,620

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)
nssv16900205<0.00116404
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