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nsv5462635

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,291

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 149 SVs from 26 studies. See in: genome view    
Submitted genomic26,248,719-26,250,009Question Mark
Overlapping variant regions from other studies: 149 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):26,248,947-26,250,237Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5462635Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr626,248,71926,250,009
nsv5462635RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr626,248,94726,250,237

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16982368deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16982368Submitted genomicNC_000006.12:g.262
48719_26250009del
GRCh38 (hg38)NC_000006.12Chr626,248,71926,250,009
nssv16982368RemappedPerfectNC_000006.11:g.262
48947_26250237del
GRCh37.p13First PassNC_000006.11Chr626,248,94726,250,237

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)
nssv16982368<0.00116404
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