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nsv5533007

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,638

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 183 SVs from 23 studies. See in: genome view    
Submitted genomic36,225,669-36,229,306Question Mark
Overlapping variant regions from other studies: 183 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):33,805,632-33,809,269Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5533007Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1836,225,66936,229,306
nsv5533007RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1833,805,63233,809,269

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17717354deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17717354Submitted genomicNC_000018.10:g.362
25669_36229306del
GRCh38 (hg38)NC_000018.10Chr1836,225,66936,229,306
nssv17717354RemappedPerfectNC_000018.9:g.3380
5632_33809269del
GRCh37.p13First PassNC_000018.9Chr1833,805,63233,809,269

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)
nssv17717354<0.00126404
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