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nsv5509313

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:163

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 136 SVs from 33 studies. See in: genome view    
Submitted genomic67,683,431-67,683,593Question Mark
Overlapping variant regions from other studies: 136 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):67,450,902-67,451,064Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5509313Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1167,683,43167,683,593
nsv5509313RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1167,450,90267,451,064

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17046265deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17046265Submitted genomicNC_000011.10:g.676
83431_67683593del
GRCh38 (hg38)NC_000011.10Chr1167,683,43167,683,593
nssv17046265RemappedPerfectNC_000011.9:g.6745
0902_67451064del
GRCh37.p13First PassNC_000011.9Chr1167,450,90267,451,064

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)
nssv17046265<0.00136404
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