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nsv5514258

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,007

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 172 SVs from 41 studies. See in: genome view    
Submitted genomic69,738,102-69,741,108Question Mark
Overlapping variant regions from other studies: 172 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):69,772,005-69,775,011Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5514258Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1669,738,10269,741,108
nsv5514258RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1669,772,00569,775,011

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17707139deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17707139Submitted genomicNC_000016.10:g.697
38102_69741108del
GRCh38 (hg38)NC_000016.10Chr1669,738,10269,741,108
nssv17707139RemappedPerfectNC_000016.9:g.6977
2005_69775011del
GRCh37.p13First PassNC_000016.9Chr1669,772,00569,775,011

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)
nssv17707139<0.00116404
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