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nsv5425825

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:43

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 120 SVs from 26 studies. See in: genome view    
Submitted genomic9,839,404-9,839,446Question Mark
Overlapping variant regions from other studies: 121 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):9,992,000-9,992,042Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5425825Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr129,839,4049,839,446
nsv5425825RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr129,992,0009,992,042

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17052851alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17052851Submitted genomicNC_000012.12:g.983
9404_9839446ins300
GRCh38 (hg38)NC_000012.12Chr129,839,4049,839,446
nssv17052851RemappedPerfectNC_000012.11:g.999
2000_9992042ins300
GRCh37.p13First PassNC_000012.11Chr129,992,0009,992,042

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)
nssv17052851<0.00116404
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