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nsv5466294

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,871

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 169 SVs from 39 studies. See in: genome view    
Submitted genomic26,373,488-26,380,358Question Mark
Overlapping variant regions from other studies: 169 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):26,373,716-26,380,586Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5466294Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr626,373,48826,380,358
nsv5466294RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr626,373,71626,380,586

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16982379deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16982379Submitted genomicNC_000006.12:g.263
73488_26380358del
GRCh38 (hg38)NC_000006.12Chr626,373,48826,380,358
nssv16982379RemappedPerfectNC_000006.11:g.263
73716_26380586del
GRCh37.p13First PassNC_000006.11Chr626,373,71626,380,586

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)
nssv16982379<0.00126404
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