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nsv5430190

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,584

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 219 SVs from 47 studies. See in: genome view    
Submitted genomic69,908,417-69,926,000Question Mark
Overlapping variant regions from other studies: 219 SVs from 47 studies. See in: genome view    
Remapped(Score: Perfect):70,374,100-70,391,683Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5430190Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr169,908,41769,926,000
nsv5430190RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr170,374,10070,391,683

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16904064deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16904064Submitted genomicNC_000001.11:g.699
08417_69926000del
GRCh38 (hg38)NC_000001.11Chr169,908,41769,926,000
nssv16904064RemappedPerfectNC_000001.10:g.703
74100_70391683del
GRCh37.p13First PassNC_000001.10Chr170,374,10070,391,683

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)
nssv16904064<0.00156402
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