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nsv5464405

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,084

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 103 SVs from 23 studies. See in: genome view    
Submitted genomic33,797,524-33,802,607Question Mark
Overlapping variant regions from other studies: 103 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):33,765,301-33,770,384Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5464405Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr633,797,52433,802,607
nsv5464405RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr633,765,30133,770,384

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16983557deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16983557Submitted genomicNC_000006.12:g.337
97524_33802607del
GRCh38 (hg38)NC_000006.12Chr633,797,52433,802,607
nssv16983557RemappedPerfectNC_000006.11:g.337
65301_33770384del
GRCh37.p13First PassNC_000006.11Chr633,765,30133,770,384

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)
nssv16983557<0.00116404
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