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nsv5558104

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 248 SVs from 45 studies. See in: genome view    
Submitted genomic25,339,359-25,339,410Question Mark
Overlapping variant regions from other studies: 248 SVs from 45 studies. See in: genome view    
Remapped(Score: Perfect):25,665,850-25,665,901Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5558104Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr125,339,35925,339,410
nsv5558104RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr125,665,85025,665,901

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16900201sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16900201Submitted genomicNC_000001.11:g.253
39359_25339410ins1
94
GRCh38 (hg38)NC_000001.11Chr125,339,35925,339,410
nssv16900201RemappedPerfectNC_000001.10:g.256
65850_25665901ins1
94
GRCh37.p13First PassNC_000001.10Chr125,665,85025,665,901

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)
nssv16900201<0.00116404
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