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nsv5525042

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 171 SVs from 37 studies. See in: genome view    
Submitted genomic5,029,297-5,029,348Question Mark
Overlapping variant regions from other studies: 171 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):5,079,298-5,079,349Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5525042Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr165,029,2975,029,348
nsv5525042RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr165,079,2985,079,349

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17704858deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17704858Submitted genomicNC_000016.10:g.502
9297_5029348del
GRCh38 (hg38)NC_000016.10Chr165,029,2975,029,348
nssv17704858RemappedPerfectNC_000016.9:g.5079
298_5079349del
GRCh37.p13First PassNC_000016.9Chr165,079,2985,079,349

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)
nssv177048580.0352246404
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