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nsv6289766

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 84 SVs from 22 studies. See in: genome view    
Submitted genomic26,060,912-26,060,912Question Mark
Overlapping variant regions from other studies: 84 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):26,456,878-26,456,878Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6289766Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2226,060,91226,060,912
nsv6289766RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2226,456,87826,456,878

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17941294insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17941294Submitted genomicNC_000022.11:g.260
60912_26060913ins6
1
GRCh38 (hg38)NC_000022.11Chr2226,060,91226,060,912
nssv17941294RemappedPerfectNC_000022.10:g.264
56878_26456879ins6
1
GRCh37.p13First PassNC_000022.10Chr2226,456,87826,456,878

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)
nssv179412940.041801936
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